Sharplight Technologies, Ltd. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Sharplight Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Omnimax S3, Omnimax S4, Rapid Family, DERMATOLOGICAL TREATMENT DEVICE FAMILY
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.
510(k) submissions have been managed by Ilan Sharon as regulatory consultant.
FDA 510(k) Regulatory Record - 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