Medical Device Manufacturer · US , Chicago , IL

Derma-Lase Co. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Derma-Lase Co. has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 5 cleared submissions from 1992 to 1993. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Derma-Lase Co. Filter by specialty or product code using the sidebar.

Derma-Lase Co. 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 - Derma-Lase Co.

5 devices

1-5 of 5