Stiefel Laboratories, Inc. is one of 23364 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stiefel Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IMPRUV A.I. CREAM WOUND AND SKIN EMULSION
1
Total
1
Cleared
0
Denied
Stiefel Laboratories, Inc. is a dermatology and wound care company with a manufacturing facility in Oak Hill, US. The company specializes in topical formulations for skin health and wound management.
Stiefel Laboratories received 1 FDA 510(k) clearance from 1 total submission, with its cleared device in the General & Plastic Surgery category. The company's regulatory activity dates to 2005. As a historical record, Stiefel Laboratories is no longer active in FDA submissions.
The company's cleared device, IMPRUV A.I. CREAM WOUND AND SKIN EMULSION, represents its focus on advanced wound and skin care solutions. Explore the device name, product code, and clearance details in the 510(k) database.
FDA 510(k) Regulatory Record - Stiefel Laboratories, Inc.
1 devices