Medical Device Manufacturer · US , Mchenry , IL

Neward Enterprises, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

Total

Cleared

Denied

Neward Enterprises, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1984 to 1996. Primary specialty: Obstetrics & Gynecology.

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

Neward Enterprises, 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 - Neward Enterprises, Inc.

8 devices

1-8 of 8