Medical Device Manufacturer · US , Dover , NJ

Keilei Intl., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1989

Total

Cleared

Denied

Keilei Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Dover, US.

Historical record: 5 cleared submissions from 1989 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Keilei Intl., Inc. Filter by specialty or product code using the sidebar.

Keilei Intl., Inc. 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 - Keilei Intl., Inc.

5 devices

1-5 of 5