Medical Device Manufacturer · US , Park Forest , IL

Adri - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1987

Total

Cleared

Denied

Adri has 5 FDA 510(k) cleared medical devices. Based in Park Forest, US.

Historical record: 5 cleared submissions from 1987 to 2004. Primary specialty: General & Plastic Surgery.

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

Adri 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 - Adri

6 devices

1-6 of 6