Verticor, Ltd. v. Michael Wood , 2015 Tex. App. LEXIS 11722 ( 2015 )


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  •       TEXAS COURT OF APPEALS, THIRD DISTRICT, AT AUSTIN
    NO. 03-14-00277-CV
    Verticor, Ltd., Appellant
    v.
    Michael Wood, Appellee
    FROM THE DISTRICT COURT OF TRAVIS COUNTY, 419TH JUDICIAL DISTRICT
    NO. D-1-GN-13-002432, HONORABLE AMY CLARK MEACHUM, JUDGE PRESIDING
    OPINION
    The pivotal issue in this appeal—one of first impression for this Court—is whether
    personal-injury claims asserted against the manufacturer of a medical device are “health care liability
    claims” within the meaning of the Texas Medical Liability Act (TMLA). At least on this record, we
    hold they are not.
    BACKGROUND
    The underlying dispute arises from surgery performed on appellee Michael Wood
    by James Hansen, M.D., to treat a herniated disc in Wood’s lumbar region. As part of the procedure,
    Dr. Hansen inserted into Wood’s spine a device known as the “Eclipse Sphere” that was
    manufactured by Verticor, Ltd., the appellant here. Complications subsequently developed, and
    Wood eventually sued both Dr. Hansen and Verticor for money damages.
    Wood’s liability theories center primarily on a contention that Dr. Hansen used
    the Eclipse Sphere in a “motion-sparing, non-fusion” surgical procedure even though the federal
    Food and Drug Administration had cleared the device solely for use in “lumbar intervertebral fusion
    procedures” and required that a warning be placed on all product packaging and surgical manuals
    stating that “the safety and effectiveness of this device for use in motion-sparing non-fusion
    procedures has not been established.”1 Wood alleges in part that Dr. Hansen acted with professional
    negligence and gross negligence in performing this “off-label” and “experimental” procedure
    and in failing to obtain Wood’s informed consent to it. Wood further complains that Verticor
    solicited Dr. Hansen’s “off-label” use of the Eclipse Sphere and failed to disclose the FDA warning
    adequately, seeking recovery based on theories of strict product liability for “marketing defect,”
    negligent marketing of the device, and breach of the implied warranty of merchantability. Wood
    additionally claims that both defendants engaged in a “fraudulent” scheme whereby Verticor made
    “secret payments” or “kickbacks” to Dr. Hansen to induce his “off-label” uses of the device.
    The merits of Wood’s allegations are not yet before us—instead, we are called upon
    only to consider the extent to which his claims implicate the requirements and limitations of
    the TMLA. The TMLA imposes several substantive and procedural constraints on the prosecution
    of “health care liability claims” (HCLCs), including damage caps2 and the now-familiar (and often-
    litigated) requirement that a plaintiff must serve one or more “expert reports” as to “each physician
    1
    Wood elaborates that the FDA, which regulates the market entry of new medical devices,
    cleared the Eclipse Sphere for sale through its “510(k)” premarket notification process, an
    exception to the agency’s more rigorous premarket approval requirements that is tied to the device’s
    “substantial equivalence” to a pre-existing device. See generally Medtronic, Inc. v. Lohr, 
    518 U.S. 470
    , 476–80 (1996) (summarizing the regulatory regime).
    2
    See Tex. Civ. Prac. & Rem. Code §§ 74.301–.303.
    2
    or health care provider against whom a liability claim is asserted” early in the suit or else face
    dismissal of that claim, with fee shifting, upon motion of that defendant.3 The TMLA defines a
    “health care liability claim” as:
    a cause of action against a health care provider or physician for
    treatment, lack of treatment, or other claimed departure from
    accepted standards of medical care, or health care, or safety or
    professional or administrative services directly related to health care,
    which proximately results in injury or death of a claimant, whether
    the claimant’s claim or cause of action sounds in tort or contract.4
    One implication of this definition, important for this case, is that “only claims brought against
    physicians and health care providers may qualify as health care liability claims.”5
    Wood has acknowledged that he asserted one or more HCLCs against Dr. Hansen,
    a physician, and has, accordingly, served what is intended to be a TMLA-compliant “expert report”
    regarding that defendant. As to Verticor, however, Wood has insisted that his claims each fall
    3
    
    Id. § 74.351(a),
    (b); see Randol Mill Pharmacy v. Miller, 
    465 S.W.3d 612
    , 615–16
    (Tex. 2015). To be precise, the expert-report requirement applies to a “claimant” who asserts an
    HCLC, but “claimant” for present purposes is merely synonymous with a plaintiff who asserts such a
    claim. See Tex. Civ. Prac. & Rem. Code § 74.001(a)(2) (defining “claimant” as “a person, including
    a decedent’s estate, seeking or who has sought recovery of damages in a health care liability claim”).
    Consequently, there is no dispute here that Wood would be a “claimant” for purposes of the TMLA’s
    expert-report requirement to the extent his claims qualify as HCLCs.
    
    4 Tex. Civ
    . Prac. & Rem. Code § 74.001(a)(13).
    5
    Randol Mill 
    Pharmacy, 465 S.W.3d at 616
    (quoting Tex. Civ. Prac. & Rem. Code
    § 74.001(a)(13)); see also Texas West Oaks Hosp., LP v. Williams, 
    371 S.W.3d 171
    , 179–80
    (Tex. 2012) (“An HCLC contains three basic elements: (1) a physician or health care provider must
    be a defendant; (2) the claim or claims at issue must concern treatment, lack of treatment, or a
    departure from accepted standards of medical care, or health care, or safety or professional or
    administrative services directly related to health care; and (3) the defendant’s act or omission
    complained of must proximately cause the injury to the claimant.”).
    3
    outside the TMLA’s definition of an HCLC and, in turn, are not subject to the Act’s procedures
    and limitations. That issue was initially raised by Verticor in its answer, in which it pleaded, as an
    affirmative defense, that “Verticor is a healthcare provider as defined by statute and case law” and
    that “[Wood’s] claims are, in reality, healthcare liability claims as that term is defined by [the
    TMLA].” Verticor’s pleading prompted Wood to move for partial summary judgment that Verticor
    is not a “health care provider” as defined by the TMLA (a conclusion that, again, would also mean
    that his claims against Verticor could not be HCLCs).6
    In his summary-judgment motion, Wood asserted no-evidence grounds challenging
    whether Verticor could present evidence that it met any component of the TMLA’s definition of
    “health care provider.” That definition states as follows:
    (A)     “Health care provider” means any person, partnership, professional
    association, corporation, facility, or institution duly licensed, certified,
    registered, or chartered by the State of Texas to provide health care,
    including:
    (i)     a registered nurse;
    (ii)    a dentist;
    (iii)   a podiatrist;
    (iv)    a pharmacist;
    (v)     a chiropractor;
    (vi)    an optometrist;
    6
    See Randol Mill 
    Pharmacy, 465 S.W.3d at 616
    (quoting Tex. Civ. Prac. & Rem. Code
    § 74.001(a)(13)). There has been no contention that Verticor is a physician, so Wood’s claims
    against it could be HCLCs only if (1) Verticor is a “health care provider” and (2) the other elements
    of an HCLC definition are also satisfied.
    4
    (vii)   a health care institution; or
    (viii) a health care collaborative certified under Chapter 848, Insurance
    Code.
    (B)      The term includes:
    (i)     an officer, director, shareholder, member, partner, manager, owner,
    or affiliate of a health care provider or physician; and
    (ii)    an employee, independent contractor, or agent of a health care
    provider or physician acting in the course and scope of the
    employment or contractual relationship.7
    Wood also asserted “traditional” grounds seeking to negate certain of the definition’s components
    with evidence that consisted of Verticor’s responses to requests for admissions. In them, Verticor
    had admitted that, inter alia, none of its principals or employees is a registered nurse, dentist,
    podiatrist, pharmacist, chiropractor, or optometrist;8 that neither “Verticor nor any of its employees
    performed any act or furnished any treatment to [Wood];” and that “Verticor is not licensed to
    perform healthcare.”
    In response to Wood’s no-evidence grounds, Verticor joined issue only with
    respect to the portion of the definition’s paragraph (A) that refers generally to a “person, partnership,
    professional association, corporation, facility, or institution duly licensed, certified, registered, or
    chartered by the State of Texas to provide health care.” As evidence that it met that requirement,
    Verticor relied solely on proof that it had operated at relevant times under a “device manufacturer”
    
    7 Tex. Civ
    . Prac. & Rem. Code § 74.001(a)(12).
    8
    Verticor similarly admitted that none of its principals or employees holds “any advanced
    degree in the medical or healthcare field.”
    5
    license issued by the Texas Department of State Health Services.9 Verticor likewise denied that it
    had conceded the issue through its admissions that it “is not licensed to perform health care” or that
    neither it nor any employee had “performed any act or furnished any treatment to [Wood].” What
    the TMLA’s definition of “health care provider” actually required, Verticor urged, was that it be
    “licensed . . . to provide health care,” not that it be licensed to perform any procedure or treatment
    directly on Wood. It was “licensed . . . to provide health care,” Verticor insisted, because it was
    licensed to manufacture a medical device that is used in and integral to medical procedures that
    physicians like Dr. Hansen perform on patients like Wood.
    The district court granted Wood’s motion for partial summary judgment without
    specifying the grounds on which it relied. Subsequently, Verticor moved for reconsideration of
    that order. Contemporaneously with this motion, Verticor filed—in its first request for affirmative
    relief based on its arguments seeking to invoke the TMLA—a motion to dismiss Wood’s claims
    against it on the basis that Wood, consistent with his position that the Act was inapplicable, had not
    timely served the “expert report” that the Act would require.10 In support of these motions, Verticor
    presented no new evidence to demonstrate that it is a “health care provider” or that the claims against
    it are “health care liability claims.”
    9
    Verticor also urged that it had not been afforded adequate opportunity for discovery, see
    Tex. R. Civ. P. 166a(i), but has not brought this complaint forward on appeal. Nor has it preserved
    any other objection regarding Wood’s no-evidence motion.
    10
    See Tex. Civ. Prac. & Rem. Code § 74.351(a), (b).
    6
    The district court denied both Verticor’s motion to reconsider the prior summary-
    judgment ruling and the new motion to dismiss.11 Verticor timely perfected an appeal from the order
    denying its motion to dismiss.12 Our statutory grant of jurisdiction over this interlocutory appeal also
    extends to reviewing the district court’s otherwise-unappealable interlocutory summary-judgment
    order, to the extent that ruling bears upon the validity of the appealable order.13
    11
    The district court had initially issued a letter indicating that it would deny Verticor’s
    motion for reconsideration but would decline to rule on Verticor’s motion to dismiss, in the view that
    its summary-judgment ruling would “moot” the expert-report issue. After Verticor objected, the
    district court proceeded also to rule on Verticor’s motion to dismiss and denied it, and the court’s
    signed order reflects both this ruling and its denial of reconsideration.
    12
    See 
    id. § 51.014(a)(9)
    (authorizing interlocutory appeal from an order that “denies all
    or part of the relief sought by a motion under Section 74.251(b)); Tex. R. App. P. 26.1(b), 28.1
    (twenty-day deadline to perfect this appeal). Although Verticor’s motion to dismiss necessarily
    turned in part on whether it was a “health care provider,” an issue already addressed in the
    district court’s earlier summary-judgment ruling, the dismissal motion marked the first occasion in
    which Verticor, in either form or substance, had sought “the relief sought by a motion under
    Section 74.241(a)”—dismissal based on Wood’s failure to file an expert report. Consequently, this
    is not a situation in which the earlier summary-judgment ruling would be deemed a “den[ial of] all
    or part of the relief sought by a motion under Section 74.251(b)” that triggered Verticor’s appellate
    deadlines and rendered untimely its appeal from the later ruling on its dismissal motion. Cf. Texas
    Cityview Care Ctr. LP v. Foster, No. 02–13–00315–CV, 
    2015 WL 736559
    , at *3 (Tex. App.—Fort
    Worth Feb. 19, 2015, no pet.) (mem. op.) (where defendant filed TMLA motion to dismiss, was
    denied, and subsequently “repackaged” motion as a “motion for summary judgment” that was also
    denied, then attempted to appeal latter ruling under Tex. Civ. Prac. & Rem. Code § 51.014(a)(9),
    appellate court lacked jurisdiction because ruling substantively was the unappealable denial of a
    motion to reconsider an order that “denies all or part of the relief sought by a motion under
    Section 74.251(b),” not an appeal from an order denying the original motion, and came too late to
    invoke appellate jurisdiction to review the order denying the original motion (citing City of Houston
    v. Estate of Jones, 
    388 S.W.3d 663
    , 667 (Tex. 2012) (analogous holdings regarding attempted
    interlocutory appeal of order denying a successive duplicative plea to the jurisdiction))). Though he
    chides Verticor for its multiple “bites at the apple” below, Wood has not asserted that the prior
    summary-judgment ruling gives rise to any jurisdictional impediment on appeal.
    13
    See Railroad Comm’n v. Air Prods. & Chems., Inc., 
    594 S.W.2d 219
    , 221–22 (Tex. Civ.
    App.—Austin 1980, writ ref’d n.r.e.) (“Non-appealable interlocutory orders cannot be attacked
    in an appeal from an appealable interlocutory order, except insofar as the question raised might
    7
    ANALYSIS
    In a single issue on appeal, Verticor urges that the district court had no discretion
    but to grant its TMLA motion to dismiss based on Wood’s failure to serve an “expert report” with
    respect to his claims against the company. Verticor cannot prevail, as it acknowledges, unless it can
    establish that it is a “health care provider” as defined by the TMLA. In the posture of this case, that
    issue turns on the meaning of a particular phrase within that definition, “licensed . . . by the State of
    Texas to provide health care.” And, as Verticor has relied solely on evidence that it holds a type of
    license from the State of Texas, a “device manufacturer” license, the issue distills further to whether
    this license means Verticor is “licensed . . . by the State of Texas to provide health care,” as the
    definition requires. Further, as framed by the proceedings below, Verticor’s argument reduces to the
    narrow proposition that it is “licensed . . . by the State of Texas to provide health care” because it
    is licensed to manufacture a medical device that is then used by another person or entity in the care
    or treatment of a patient. There is no evidence nor contention from Verticor, for example, that it had
    any involvement whatsoever in Wood’s care or treatment, or was licensed to be involved in his care
    or treatment, beyond merely manufacturing the Eclipse Shield that Dr. Hansen ultimately used in
    Wood’s surgery and placing it in the stream of commerce. In fact, Verticor’s admissions negate such
    direct or additional involvement.
    Resolution of these questions turns on construction of the TMLA, a question of
    law that we review de novo.14 Our primary objective in construing a statute is “to determine and
    affect the validity of the appealable order.” (citing State v. Cook United, Inc., 
    464 S.W.2d 105
    , 106
    (Tex. 1971); Texas State Bd. of Exam’rs in Optometry v. Carp, 
    343 S.W.2d 242
    , 234 (Tex. 1961))).
    14
    See Texas West 
    Oaks, 371 S.W.3d at 177
    (citing MCI Sales & Serv., Inc. v. Hinton,
    
    329 S.W.3d 475
    , 500 (Tex. 2010)).
    8
    give effect to the Legislature’s intent.”15 We rely on the plain meaning of the text as expressing the
    Legislature’s intent unless a different meaning is supplied by legislative definition or is apparent
    from the context, or the plain meaning leads to “absurd results” that the Legislature could not
    possibly have intended.16 Further, the Legislature has specifically instructed that “[a]ny legal term
    or word of art used in [the TMLA], not otherwise defined [therein], shall have such meaning as is
    consistent with the common law.”17 We presume the Legislature selected language in a statute with
    care and acted purposefully in including or excluding particular words and phrases.18
    Whether Verticor is “licensed . . . by the State of Texas to provide health care” turns
    in part on the meaning of “health care,” which is itself a defined term within the TMLA. “Health
    care” means “any act or treatment performed or furnished, or that should have been performed or
    furnished, by any health care provider for, to, or on behalf of a patient during the patient’s medical
    care, treatment, or confinement.”19 The crux of Verticor’s position is that it “provide[s] health care”
    under its “device manufacturer” license, and is thus a “health care provider,” because it provides the
    Eclipse Shield “for, to, or on behalf of a patient during the patient’s medical care, treatment, or
    confinement.” Verticor’s reasoning is belied by a close examination of the statutory text.
    Verticor’s argument might find stronger support if the TMLA’s “health care
    provider” definition had referred to a person “licensed . . . by the State of Texas to provide
    15
    Texas Lottery Comm’n v. First State Bank of DeQueen, 
    325 S.W.3d 628
    , 635 (Tex. 2010).
    16
    Id.
    1
    7 Tex. Civ
    . Prac. & Rem. Code § 74.001(b).
    18
    
    DeQueen, 325 S.W.3d at 635
    .
    
    19 Tex. Civ
    . Prac. & Rem. Code § 74.001(10).
    9
    products or services used in health care” or that “have some relationship to health care.” But the
    Legislature did not write the statute that way—instead, it required that a “health care provider” be
    “licensed . . . by the State of Texas to provide health care.” That phrasing indicates that Verticor’s
    license must authorize it “to provide” something that is in itself “health care.”
    As the issue is framed here, Verticor’s license authorizes it “to provide” (at least
    in the sense of manufacturing and selling) the Eclipse Sphere—and nothing more. Consequently,
    Verticor can be “licensed . . . by the State of Texas to provide health care” only if the Eclipse Sphere
    is, in itself, “health care” as the TMLA defines that term. That definition defies such an application.
    Under it, “health care” is distinguished by either of two nouns—“act” or “treatment”—that is
    “performed or furnished,” or should have been, “for, to, or on behalf of a patient during the patient*s
    medical care, treatment, or confinement.” The first alternative, an “act,” denotes some sort of
    deed or activity.20 As an inanimate object, the Eclipse Shield, in itself, could not be an “act,”
    although it might be utilized in acts that qualify as “health care,” such as surgery. Similarly, the
    other alternative, “treatment” also denotes some form of activity that is performed or furnished for
    or to a patient.21 Consequently, the Eclipse Shield would not, in itself, be a “treatment,” although
    it might be utilized in a “treatment.” Indeed, Verticor effectively concedes these same conclusions
    20
    See The Compact Edition of the Oxford English Dictionary 14 (2d ed. 1994) (defining
    noun “act” as a “thing done; a deed, a performance (of an intelligent being)”); American Heritage
    Dictionary of the English Language 16 (5th ed. 2011) (defining noun “act” as the “process of doing
    or performing something” and “[s]omething done or performed; a deed”).
    21
    See Black’s Law Dictionary 1731, 1732 (10th ed. 2014) (defining “treat” as “care for
    (a medical patient); to try to cure the illness or injury of (a person) by using medicine, hospital care,
    surgery, etc.” and “subject (a disease, debility, etc.) to a regimen of medicine, exercise, etc.”);
    see also Covenant Health Sys. v. Barnett, 
    342 S.W.3d 226
    , 230–31 (Tex. App.—Amarillo 2011,
    no pet.) (concluding that heart screening is within TMLA’s definition of “treatment” by referring to
    Black’s Law Dictionary and medical dictionary and citing TMLA section 74.001(b)).
    10
    through its admission that neither it nor any of its employees “performed any act or furnished any
    treatment to Wood.”
    These conclusions find further support when taking account of the broader statutory
    and jurisprudential context in which this language appears.22 Historically, Texas common law has
    distinguished between the tort duties owed by health-care practitioners, which focus on specialized
    “standards of care” that define the parameters of reasonableness in providing their services to
    patients, versus the duties owed by the manufacturers and sellers of the products utilized by health-
    care practitioners, which focus on the condition of the product itself or the manner in which it was
    made or sold.23 One corollary of this basic distinction, in fact, is that the “learned intermediary”
    doctrine may limit the duty of a manufacturer or seller of prescription drugs or medical devices to
    warn end users of the product’s dangerous propensities, in the view that a physician or health care
    provider who receives an adequate warning should be relied upon to convey such information to the
    end user as is appropriate under the circumstances.24 The distinction is also reflected in important
    22
    See, e.g., In re Office of Attorney Gen., 
    422 S.W.3d 623
    , 629 (Tex. 2013) (“We
    must endeavor to read the statute contextually, giving effect to every word, clause, and sentence.”);
    TGS-NOPEC Geophysical Co. v. Combs, 
    340 S.W.3d 432
    , 441 (Tex. 2011) (“Language cannot
    be interpreted apart from context. The meaning of a word that appears ambiguous when viewed
    in isolation may become clear when the word is analyzed in light of the terms that surround it.”);
    see also Texas Bd. of Chiropractic Exam’rs v. Texas Med. Ass’n, 
    375 S.W.3d 464
    , 474
    (Tex. App.—Austin 2012, pet. filed) (“We also presume that the legislature was aware of the
    background law and acted with reference to it.” (citing Acker v. Texas Water Comm’n, 
    790 S.W.2d 299
    , 301 (Tex. 1990)).
    23
    See, e.g., Ethicon , Inc. v. Parten, 
    520 S.W.2d 527
    , 532–34 (Tex. Civ. App.—Houston
    [14th Dist.] 1975, no writ) (in case involving broken surgical needle left in patient, appellate court
    resolved issues as to needle manufacturer under products-liability law and issues as to physician
    under medical-malpractice law).
    24
    See Centocor Inc. v. Hamilton, 
    372 S.W.3d 140
    , 153–70 (Tex. 2012) (extensively
    analyzing the “learned intermediary” doctrine and its underlying rationales and applying it to hold
    11
    differences between the TMLA and the statutory scheme the Legislature has addressed to claims
    arising from the allegedly defective condition of products.
    In 1993, the Legislature enacted Chapter 82 of the Civil Practice and Remedies Code
    to impose certain limitations upon “products liability actions,”25 defined as those asserted against
    a “manufacturer” or “seller” for recovery of personal injuries or property damage “allegedly
    caused by a defective product whether that action is based on strict tort liability, strict products
    liability, negligence, misrepresentation, breach of express or implied warranty, or any other theory
    or combination of theories.”26 A “manufacturer” is defined as “a designer, formulator, constructor,
    rebuilder, fabricator, producer, compounder, processor, or assembler of any product or any
    component part thereof and who places [it] in the stream of commerce,”27 while a “seller” is “a
    person engaged in the business of distributing or otherwise placing, for any commercial purpose, in
    the stream of commerce for use or consumption a product or any component part thereof.”28 In
    contrast to Chapter 82*s concern with liability arising from the allegedly deficient condition of
    products, the TMLA is focused on liability arising from the allegedly deficient quality of services
    provided to a patient. Among other examples, the TMLA requires that any expert who gives
    that drug manufacturer satisfied duty to warn end users of product’s dangerous propensities by
    providing warnings to prescribing physician); Bean v. Baxter Healthcare Corp., 
    965 S.W.2d 656
    ,
    663 (Tex. App.—Houston [14th Dist.] 1998, no pet.) (applying doctrine to benefit of breast-implant
    manufacturer where entity provided warnings to physicians).
    25
    See Act of Feb. 24, 1993, 73d Leg., R.S., ch. 5, §§ 1–5, 1993 Tex. Gen. Laws 13 (codified
    at Tex. Civ. Prac. & Rem. Code §§ 82.001–.008).
    
    26 Tex. Civ
    . Prac. & Rem. Code § 82.001(2).
    27
    
    Id. § 82.001(4).
           28
    
    Id. § 82.001(3).
    12
    testimony regarding the standard of care must have knowledge of “accepted standards” of “medical
    care” or “health care” “for the diagnosis, care, or treatment of the illness, injury, or condition
    involved in the claim.”29 Against this backdrop, it would hardly be surprising that the Legislature
    would define “health care” under the TMLA in terms of “acts” and “treatments,” as opposed to
    products or things.30
    This understanding of “health care” also comports with the common usage of that
    term. While statutory definitions in theory trump the ordinary meaning of the terms being defined,
    the Texas Supreme Court has also instructed us to “presume that the definition of a common word
    accords with and does not conflict with the ordinary meaning unless the language clearly indicates
    otherwise.”31 In common usage, one associates “health care” with medical intervention, assistance,
    or other acts—e.g., one’s family doctor performing an annual physical or a nurse administering a
    flu shot—as opposed to the mere making or selling of a product used in providing such services.32
    Focusing as it does on acts and treatment provided to patients, the TMLA’s definition of “health
    care” does not clearly depart from this basic notion.
    Nor does the Act’s definition of “health care provider” clearly depart from that
    meaning. The TMLA’s definition, again, refers to persons or entities who are “duly licensed,
    29
    
    Id. §§ 74.401(a)(2),
    .402(b)(2).
    30
    
    Id. § 74.001(10).
           31
    In re Ford Motor Co., 
    442 S.W.3d 265
    , 271 & n.20 (Tex. 2014) (citing Antonin Scalia &
    Bryan A. Garner, Reading Law 232 (2012)).
    32
    See, e.g., American Heritage Dictionary at 810 (defining “health care” as “prevention,
    treatment, and management of illness and the preservation of mental and physical well-being through
    the services offered by the medical and allied health professions”).
    13
    certified, registered, or chartered by the State of Texas to provide health care,” and goes on to cite
    several specific examples.33 While these exemplars are non-exclusive,34 they nonetheless tend to
    confirm that the Legislature had in mind the sorts of trained professionals that provide or perform
    the sorts of acts that one ordinarily associates with “health care”—e.g., registered nurses, dentists,
    podiatrists, chiropractors, optometrists, and “health care institutions,”35 a term that includes the likes
    of hospitals, ambulatory surgical centers, hospice, and nursing homes.36 This is not the sort of text
    the Legislature would use if it intended to transform ordinary notions of “health care” or “health care
    provider” to include persons or entities whose only involvement in patient care is to provide some
    product or device used in that process.
    That is not to say, however, that the acts or treatments distinguishing “health care”
    or “health care providers” under the TMLA cannot ever encompass some element of product
    manufacture or sale that would implicate Chapter 82, or vice versa. In Chapter 82, for example, the
    Legislature contemplated that the defendants in a “products liability action alleging that an injury
    was caused by a failure to provide adequate warnings or information with regard to pharmaceutical
    33
    See Tex. Civ. Prac. & Rem. Code § 74.001(a)(12).
    34
    See 
    id. (preceding list
    of examples with “including”); Tex. Gov’t Code § 311.005(13)
    (Code Construction Act provision stating that “‘[i]ncludes’ and ‘including’ are terms of enlargement
    and not of limitation or exclusive enumeration, and use of the terms does not create a presumption
    that components not expressed are excluded”). Accord, e.g., San Antonio Extended Med. Care, Inc.
    v. Vasquez, 
    327 S.W.3d 193
    , 197–98 (Tex. App.—San Antonio 2010, no pet.) (reaching the same
    conclusion); see also Texas West 
    Oaks, 371 S.W.3d at 179
    (stating that use of “including” in
    TMLA’s definition of “claimant” “renders any components of the definition nonexclusive” (citing
    Tex. Gov’t Code § 311.005(13); In re Allcat Claims Serv., L.P., 
    356 S.W.3d 455
    , 468 (Tex. 2011);
    Entergy Gulf States, Inc. v. Summers, 
    282 S.W.3d 433
    , 440–41 (Tex. 2009)).
    35
    See Tex. Civ. Prac. & Rem. Code § 74.001(a)(12).
    36
    See 
    id. § 74.001(a)(11).
    14
    products” may potentially include “a health care provider,” although the statute does not purport
    to adopt the TMLA’s definition of that term.37 Similarly, within the TMLA, the Legislature saw fit
    to craft a specific definition of “pharmacist” (one of the exemplars cited in the Act’s “health care
    provider” definition)38 that serves to distinguish between HCLCs arising from pharmacists’
    “dispensing of prescription medicines” under their licenses, which are made subject to the Act,
    versus claims arising from their “manufacture” of medications or “other cause of action that may
    exist at common law against them, including but not limited to [those] for the sale of mishandled or
    defective products,” which are excluded.39 And some of our sister courts have held that persons or
    entities operating under licenses similar to Verticor’s can, in some circumstances, fall within “health
    care providers” under the TMLA.40
    From the latter group of cases, Verticor distills the broad proposition that “medical
    device manufacturers—like Verticor—are health care providers under the TMLA.” In response,
    Wood urges that the opposite is true, referring us to cases that have appeared to assume that product-
    liability claims against medical-device manufacturers are governed by Chapter 82 to the exclusion
    37
    See 
    id. § 82.007(a).
           38
    See 
    id. § 74.001(a)(12)(A)(iv).
           39
    
    Id. § 74.001(a)(22);
    see Randol Mill 
    Pharmacy, 465 S.W.3d at 617
    –23 (analyzing
    application of definition to compounding pharmacies and concluding that claims arising from
    compounding of pharmaceuticals were HCLCs).
    40
    See Strobel v. Marlow, 
    341 S.W.3d 470
    (Tex. App.—Dallas 2011, no pet.); 
    Vasquez, 327 S.W.3d at 198
    –99; Perkins v. Apria Healthcare, Inc., 3:10-CV-2295-D, 
    2012 WL 4928895
    ,
    at *3–4 (N.D. Tex. Oct. 17, 2012).
    15
    of the TMLA.41 The true picture, as we have already suggested, is more complicated than either of
    these diametrically opposing views.
    In the alternative, Wood urges that the cases on which Verticor relies are
    distinguishable. Those cases, Wood maintains, involve instances in which the scope of the medical-
    device manufacturer’s licensed authority was shown to extend to the provision of acts or treatment
    that would plainly be “health care” under the TMLA’s definition, as contrasted with the situation
    here, where a defendant relies on the authority to manufacture or sell a medical product. We agree
    with Wood. In Strobel, for example, the manufacturer in question was a prosthetist licensed under
    the Orthotics and Prosthetics Act42 to custom fabricate or fit medical devices to replace the missing
    limbs of specific patients.43 Further, there was evidence that the license extended to providing direct
    patient care,44 plainly acts or treatment that would characterize “health care” under the TMLA.
    Similarly, in Vasquez, the San Antonio Court of Appeals emphasized proof that the licensee was
    authorized by the Department of State Health Services to manufacture and distribute oxygen, a
    regulated drug requiring a prescription, and that its authority extended to supplying doctor-prescribed
    41
    In re Temple, 
    239 S.W.3d 885
    , 889 (Tex. App.—Texarkana 2007, no pet.) (“Claims
    regarding products liability or negligent manufacture—even when those items are medical
    devices—are not expressly or impliedly covered by Chapter 74.”); accord Meredith v. NuVasive,
    Inc., No. A-13-CA-208-SS, slip op. at 7 (W.D. Tex. Dec. 9, 2013) (citing 
    Temple, 239 S.W.3d at 889
    , to support its conclusion that, in Texas, products liability claims are distinguishable from
    health care liability claims, even where negligence theories are involved).
    42
    See 
    Strobel, 341 S.W.3d at 474
    ; see also Tex. Occ. Code §§ 605.001–.411 (Act).
    43
    See Tex. Occ. Code § 605.002(8) (defining “Licensed prosthetist”), (17) (defining
    “Prosthesis”), (18) (defining “Prosthetics”).
    44
    See 
    id. § 605.002(16)
    (“Orthotic and prosthetic services include direct patient care,
    including consultation, evaluation, treatment, education, and advice to maximize the rehabilitation
    potential of disabled individuals.”); 
    Strobel, 341 S.W.3d at 475
    –76.
    16
    “oxygen therapy” to a patient in his home, including setting the flow rate for the oxygen tanks.45 At
    most, these authorities would refute the categorical notion that medical-device manufacturers can
    never be “health care providers.” They fall far short of demonstrating that the mere manufacture
    and sale of a medical device ipso facto constitutes the provision of “health care” under the TMLA,
    as Verticor argues.
    Without more, Verticor has not raised a fact issue, let alone demonstrated
    conclusively, that it is a “health care provider” under the TMLA. Consequently, Wood’s claims
    against it cannot be HCLCs, and the district court did not err in denying Verticor’s motion to
    dismiss. We overrule Verticor’s issue on appeal.
    CONCLUSION
    We affirm the district court’s order denying Verticor’s motion to dismiss Wood’s
    claims against it.
    __________________________________________
    Bob Pemberton, Justice
    Before Justices Puryear, Pemberton, and Field
    Affirmed
    Filed: November 13, 2015
    45
    
    Vasquez, 327 S.W.3d at 198
    –99. As for the remaining case cited by Verticor, Perkins, it
    is factually similar to Vasquez and, as such, relies on its holding. See Perkins, 
    2012 WL 4928895
    ,
    at *5.
    17