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

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

4 submissions · 4 cleared · Since 1994
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Epilady 2000, LLC General & Plastic Surgery ✕
3 devices
1-3 of 3
Cleared Jan 27, 2024
Epilaser Pro
K233224 · GEX
General & Plastic Surgery · 121d
Cleared Dec 13, 2022
Epilaser Absolute
K213105 · GEX
General & Plastic Surgery · 445d
Cleared Sep 01, 2017
Epilaser
K170970 · GEX
General & Plastic Surgery · 154d
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