Medical Device Manufacturer · US , Cherry Hill , NJ

F.M. Wiest USA, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1986

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - F.M. Wiest USA, Inc. Orthopedic ✕

3 devices

1-3 of 3

Cleared Sep 29, 1987

ARTHRO AUTOMAT 5002

Orthopedic · 188d

Cleared Sep 29, 1987

ARTHROCOMBI 5003

Orthopedic · 188d

Cleared Apr 20, 1987

Orthopedic · 117d