Medical Device Manufacturer · US , Lakewood Ranch , FL

Vilex IN Tennessee, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2014

Total

Cleared

Denied

Vilex IN Tennessee, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lakewood Ranch, US.

Historical record: 7 cleared submissions from 2014 to 2019. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Vilex IN Tennessee, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Vilex, Inc. as regulatory consultant.

Vilex IN Tennessee, Inc. is one of 13233 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vilex IN Tennessee, Inc.

7 devices

1-7 of 7