Medical Device Manufacturer · US , New Port Richey , FL

Bergen Mfg. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1986

Total

Cleared

Denied

Bergen Mfg. has 4 FDA 510(k) cleared medical devices. Based in New Port Richey, US.

Historical record: 4 cleared submissions from 1986 to 1997. Primary specialty: General & Plastic Surgery.

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

Bergen Mfg. 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 - Bergen Mfg.

4 devices

1-4 of 4