Epilady 2000, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
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.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
4 devices