Beiersdorf AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beiersdorf AG - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Beiersdorf AG has 3 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 3 cleared submissions from 2002 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Beiersdorf AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beiersdorf AG
3 devices