Aguila v. RQM+ LLC

CourtDistrict Court, S.D. Florida
DecidedAugust 12, 2025
Docket1:23-cv-24702
StatusUnknown

This text of Aguila v. RQM+ LLC (Aguila v. RQM+ LLC) is published on Counsel Stack Legal Research, covering District Court, S.D. Florida primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Aguila v. RQM+ LLC, (S.D. Fla. 2025).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF FLORIDA

CASE NO. 23-24702-CIV-DAMIAN

RAFAEL AGUILA and ACCELERATED DEVICE APPROVAL SERVICES,

Plaintiffs,

v.

RQM+ LLC, HEADSAFE MFG PTY LTD, CRYPTYCH PTY LTD, and GREG ROGER,

Defendants. _________________________________________/

ORDER ON DEFENDANT HEADSAFE MFG PTY LTD’S MOTION TO QUASH SERVICE OF PROCESS AND MOTION TO DISMISS [ECF NO. 34]

THIS CAUSE is before the Court on Defendant Headsafe Mfg Pty Ltd.’s (“Headsafe” or “Defendant”), Motion to Quash Service of Process and Motion to Dismiss [ECF No. 34 (“Motion”)], filed January 26, 2024. THE COURT has reviewed the Motion, the parties’ briefing [ECF Nos. 45 (“Response”) and 48 (“Reply”)], the pertinent portions of the record, including the declaration submitted in support of the Motion, and relevant authorities, and is otherwise fully advised. For the reasons set forth below, the Motion is due to be granted in part. I. BACKGROUND A. Relevant Factual Allegations In The First Amended Complaint. The relevant facts summarized below are taken from the allegations in the First Amended Complaint [ECF No. 1-3 at 6–56 (“Am. Compl.”)].1

1 The Court uses the pagination generated by the electronic CM/ECF database, which appears in the headers of all court filings. Plaintiffs, Rafael Aguila (“Aguila”) and Accelerated Device Approval Services (“ADAS”) (collectively, “Plaintiffs”), are in the business of medical device evaluations. ADAS is a sole proprietorship owned by Aguila. Am. Compl. ¶ 4. This action arises out of the business interaction among Plaintiffs and Defendants, RQM+ LLC (“RQM+”),2

Headsafe Mfg. Pty. Ltd. (“Headsafe”), Cryptych Pty. Ltd. (“Cryptych”), and Greg Roger (“Roger”) (collectively, the “Defendants”), in connection with third-party medical device review services. See generally Am. Compl. Between 2018 and 2021, ADAS operated as a third-party review organization accredited by the Center for Devices and Radiological Health (“CDRH”), a branch of the U.S. Food and Drug Administration (“FDA”) responsible for the regulatory oversight of medical devices, including the review and approval of 510(k) submissions.3 Am. Compl. ¶¶ 3–4. Through its CDRH-accreditation, ADAS was primarily responsible for reviewing new medical device applications and recommending to the CDRH whether the subject medical devices should be approved or not. Id. ¶ 4.

Defendant Headsafe, an Australian corporation, is the developer and legal manufacturer of NuroChek, a medical device used for electroencephalogram (EEG) analysis. Id. ¶ 16. In January 2019, Defendant Cryptych, also an Australian corporation, engaged in a partnership with Headsafe to co-develop the NuroChek device. Id. ¶¶ 8; 30. Defendant Roger,

2 In the Notice of Removal, RQM+ indicates there is no legal entity by the name “RQM+ LLC” and that, upon information and belief, Plaintiffs intended to sue Regulatory and Quality Solutions, LLC. So, for simplicity’s sake, Defendant will be referred to as RQM+ herein.

3 As alleged in the Amended Complaint, 510(k) submissions are “comprehensive dossiers that include detailed information, safety test reports, technical specifications, supporting scientific data, and evidence demonstrating that the new device is at least as safe and effective as a predicate device, an existing, legally marketed device.” Am. Compl. ¶ 4. an individual residing in Australia, is the Chief Executive Officer of Cryptych. Id. ¶ 9. Plaintiffs allege that on April 16, 2019, Defendant Cryptych entered into a contract with ADAS pursuant to which ADAS would provide third-party medical device review services to Cryptych in connection with the CDRH’s review of the NuroChek device’s 510(k)

submission. Id. ¶¶ 17, 30–31. Defendant RQM+ is a limited liability company based in Pennsylvania that specializes in consulting services for regulatory approvals of new medical devices. Id. ¶ 6. Plaintiffs allege that RQM+ served as the authorized U.S. agent for Defendants Headsafe, Cryptych, and Roger. Id. As Plaintiffs allege in the Amended Complaint, non-party Allison Komiyama (“Ms. Komiyama”) was a regulatory consultant for Defendants Cryptych, Headsafe, and Roger, and was primarily tasked with facilitating the CDRH approval of the NuroChek device. Id. Plaintiffs allege that, at the time the parties were engaged in the regulatory review process for the NuroChek device, Ms. Komiyama was employed by non-party AcKnowledge

Regulatory Services (“AcKnowledge”), which was later acquired by Defendant RQM+ in December 2021. Id. ¶ 61. Notably, according to the Amended Complaint, the NuroChek device was officially approved by the CDRH on April 23, 2020. Id. ¶ 8. Plaintiffs allege that during the course of the regulatory review process for the NuroChek device, Defendants made false representations to the CDRH about Plaintiffs’ business conduct. See generally Am. Compl. ¶¶ 16–29, 58–91. Specifically, Plaintiffs allege that Defendants “misrepresented to the CDRH the nature of the Plaintiffs’ review process, falsely suggesting that the Plaintiffs had led [Defendants] to believe that the CDRH was directly reviewing the NuroChek’s 510(k) application before its actual submission date.” Id. ¶ 108.

According to Plaintiffs, these false representations “were a significant factor in the CDRH’s eventual decision to withdraw ADAS’s accreditation as a Third-Party Review organization[.]” Id. B. The State Court Proceedings. On September 26, 2023, Plaintiffs, proceeding pro se,4 filed a Complaint in the Eleventh

Judicial Circuit Court in Miami-Dade County, Florida, against Defendants asserting claims for violation of Florida’s Security of Communications Act, defamation, tortious interference with business relations, business disparagement, fraud/fraudulent misrepresentation, negligent misrepresentation, breach of contract, and product liability. See generally ECF No. 1-2 at 5–11. On November 21, 2023, while the action was pending in state court and before the Defendants were served with the Complaint, Plaintiffs filed a “Motion to Amend Complaint” requesting leave to amend their pleading as a matter of course. Id. at 38–40. Plaintiffs attached the proposed First Amended Complaint to their Motion. Id. at 42–92. In the First Amended

Complaint, the operative pleading, Plaintiffs assert five claims against the Defendants: (1) Racial Discrimination in Medical Device Safety Testing in violation of the Florida Civil Rights Act (“FCRA”) of 1992 (Fla. Stat. § 760.01, et seq.) and the Florida Patient’s Bill of Rights and Responsibilities (“FPBRR”) (Fla. Stat. § 381.026(4)(d)(1)); (2) Fraudulent Misrepresentation; (3) Breach of Contract (solely against Cryptych); (4) Tortious Interference with Business Relations; and (5) Violation of the Florida Security of Communications Act

4 The Court notes that ADAS is a sole proprietorship owned by Aguila and, therefore, may proceed pro se. [ECF No. 1-2 at 43]. See, e.g., National Independent Theatre Exhibitors, Inc. v. Buena Vista Distrib. Co., 748 F.2d 602, 610 (11th Cir. 1984) (“As a sole proprietor, he could proceed pro se . . . .”). (“FSCA”) (Fla. Stat. § 934.01 et seq.). Id. Plaintiffs seek actual and compensatory damages, as well as punitive damages. Id. at 91–92. C. The Instant Action. On December 12, 2023, RQM+ removed the action to this Court. [ECF No. 1]. In the

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Bluebook (online)
Aguila v. RQM+ LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/aguila-v-rqm-llc-flsd-2025.