Medical Device Manufacturer · US , Chicago , IL

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

7 submissions · 7 cleared · Since 1985

Total

Cleared

Denied

Daun International, Inc. has 7 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 7 cleared submissions from 1985 to 1985. Primary specialty: Physical Medicine.

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

Daun International, 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 - Daun International, Inc.

7 devices

1-7 of 7