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Data / Medical devices / United States / Voom Medical Devices, LLC

Voom Medical Devices, LLC: FDA-registered device maker in Brentwood, TN, United States, 1 510(k) clearance

Voom Medical Devices, LLC is registered with the FDA (registration 3022928161) in Brentwood, TN, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 28, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3022928161
Address
783 Old Hickory Blvd Ste 155, Brentwood, TN, United States, 37027
Owner or operator
Voom Medical Devices, LLC (10087527)
Roles
Complaint file establishment, Manufacturer, Repackager or relabeler
First device listed
March 10, 2023
Registered through
2026
Brand names listed
Irrigation Tubing Set 3.8m, REVCON Bone Fixation Screw System

Devices it lists

DeviceProduct codeClassRoleSource
Catheter, IrrigationGBX1Repackager or relabeleraccessdata.fda.gov
Screw, Fixation, BoneHWC2Complaint file establishment, Manufactureraccessdata.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
February 28, 2023K223392REVCON (TM) Screw SystemHWCSubstantially EquivalentVoom Medical Devices, Inc.accessdata.fda.gov

Compare with other makers

Updated February 28, 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.