Medical Device Manufacturer · US , East Rockaway , NY

Laivan Corp. - FDA 510(k) Cleared Devices

6 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Laivan Corp. has 2 FDA 510(k) cleared medical devices. Based in East Rockaway, US.

Historical record: 2 cleared submissions from 1988 to 1993. Primary specialty: General & Plastic Surgery.

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

Laivan 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 - Laivan Corp.

6 devices

1-6 of 6