Beiersdorf AG is one of 24510 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beiersdorf AG - FDA 510(k) Cleared Devices
Recent clearances: CURAD SILVER ACTIVE GEL BANDAGE, CURAD SILVER BANDAGE, CURAD
3
Total
3
Cleared
0
Denied
Beiersdorf AG, is a global skin care company known for iconic brands including NIVEA, Eucerin, and Hansaplast. The company operates with a manufacturing facility in North Attleboro, Massachusetts.
Beiersdorf received 3 FDA 510(k) clearances from 3 total submissions in General & Plastic Surgery devices. The company's regulatory activity spans from 2002 to 2004. This represents a historical record of FDA clearances in wound care and surgical applications.
The cleared devices include bandage and wound dressing products under the CURAD brand, reflecting the company's focus on accessible wound management solutions. Beiersdorf's regulatory submissions demonstrate expertise in topical wound care technologies.
For detailed information on specific device names, product codes, and clearance dates, review the complete 510(k) submission history.
FDA 510(k) Regulatory Record - Beiersdorf AG
3 devices