Medical Device Manufacturer · US , Carpinteria , CA

Inamed Development Co. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

Total

Cleared

Denied

Inamed Development Co. has 7 FDA 510(k) cleared medical devices. Based in Carpinteria, US.

Historical record: 7 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Inamed Development Co. Filter by specialty or product code using the sidebar.

Inamed Development Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Inamed Development Co.

7 devices

1-7 of 7