Medical Device Manufacturer · US , Louisville , KY

Dermacare - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Dermacare has 2 FDA 510(k) cleared medical devices. Based in Louisville, US.

Historical record: 2 cleared submissions from 1988 to 1989. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Dermacare Filter by specialty or product code using the sidebar.

Dermacare 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 - Dermacare

2 devices

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