Medical Device Manufacturer · IL , Zichron Yaacov

Sharplight Technologies, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2008

4

Total

4

Cleared

0

Denied

FDA 510(k) cleared devices by Sharplight Technologies, Ltd. General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared Dec 22, 2023

Omnimax S3, Omnimax S4

General & Plastic Surgery · 84d

Cleared Nov 20, 2017

General & Plastic Surgery · 52d

Cleared Dec 21, 2011

DERMATOLOGICAL TREATMENT DEVICE FAMILY

General & Plastic Surgery · 226d

Cleared Nov 10, 2008

BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY

General & Plastic Surgery · 42d