Sharplight Technologies, Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Sharplight Technologies, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Zichron Yaacov, IL.
Last cleared in 2023. Active since 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sharplight Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sharplight Technologies, Ltd.
4 devices
Cleared
Dec 22, 2023
Omnimax S3, Omnimax S4
General & Plastic Surgery
84d
Cleared
Nov 20, 2017
Rapid Family
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