Medical Device Manufacturer · US , Elk Groove Village , IL

New Eder Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

New Eder Corp. has 4 FDA 510(k) cleared medical devices. Based in Elk Groove Village, US.

Historical record: 4 cleared submissions from 1994 to 1995. Primary specialty: Obstetrics & Gynecology.

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

New Eder 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 - New Eder Corp.

4 devices

1-4 of 4