Medical Device Manufacturer · US , Addison , IL

Avent America, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

Avent America, Inc. has 4 FDA 510(k) cleared medical devices. Based in Addison, US.

Historical record: 4 cleared submissions from 1994 to 2005. Primary specialty: Obstetrics & Gynecology.

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

Avent America, 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 - Avent America, Inc.

4 devices

1-4 of 4