Medical Device Manufacturer · US , Santa Barbara , CA

Cui Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1990

Total

Cleared

Denied

Cui Corp. has 7 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.

Historical record: 7 cleared submissions from 1990 to 1991. Primary specialty: General & Plastic Surgery.

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

Cui Corp. 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 - Cui Corp.

7 devices

1-7 of 7