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Data / Medical devices / United States / Medovate LLC

Medovate LLC: FDA-registered device maker in Brownsville, TX, United States, 1 510(k) clearance

Medovate LLC is registered with the FDA (registration 3045809869) in Brownsville, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 31, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045809869
Address
200 Texas Ave, Brownsville, TX, United States, 78521
Owner or operator
Medovate LLC (10095945)
Roles
Complaint file establishment
First device listed
May 27, 2026
Registered through
2026
Brand names listed
SAFIRA

Devices it lists

DeviceProduct codeClassRoleSource
Pump, InfusionFRN2Complaint file establishmentaccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 31, 2023K230083SAFIRAFRNSubstantially EquivalentMedovate Limitedaccessdata.fda.gov

Compare with other makers

Updated October 31, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.