Medical Device Manufacturer · US , Washington D.C. , DC

Epilady 2000, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

Epilady 2000, LLC has 4 FDA 510(k) cleared medical devices. Based in Washington D.C., US.

Latest FDA clearance: Jan 2024. Active since 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Epilady 2000, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Epilady 2000, LLC

4 devices

1-4 of 4