Medical Device Manufacturer · US , Oceanside , NY

Ellman Int'L, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2005

Total

Cleared

Denied

Ellman Int'L, Inc. has 6 FDA 510(k) cleared medical devices. Based in Oceanside, US.

Historical record: 6 cleared submissions from 2005 to 2011. Primary specialty: General & Plastic Surgery.

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

Ellman Int'L, 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 - Ellman Int'L, Inc.

6 devices

1-6 of 6