Medical Device Manufacturer · US , Englewood , CO

Cochlear Americas - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2008

Recent clearances: Cochlear™ Osia® 3(I) Sound Processor, Cochlear Osia System, Instrument Case

View 21 510(k) Devices ↓

21

Total

21

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cochlear Americas General Hospital ✕

1 devices

1-1 of 1

Cleared Aug 24, 2023

Instrument Case

General Hospital · 84d