Sharplight Technologies, Ltd.

Sharplight Technologies, Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2008, most recent 2023.

Top product codes for Sharplight Technologies, Ltd.

GEX — General, Plastic Surgery4 devices

Recent clearances by Sharplight Technologies, Ltd.

K233304 — Omnimax S3, Omnimax S4Code GEX·2023-12-22
K173169 — Rapid FamilyCode GEX·2017-11-20
K111303 — DERMATOLOGICAL TREATMENT DEVICE FAMILYCode GEX·2011-12-21
K082876 — BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILYCode GEX·2008-11-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.