Medical Device Manufacturer · US , Oceanside , NY

Ellman International, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Ellman International, Inc. has 5 FDA 510(k) cleared medical devices. Based in Oceanside, US.

Historical record: 5 cleared submissions from 2006 to 2014. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Ellman International, Inc.

5 devices

1-5 of 5