Wontech Co., Ltd.
Wontech Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2025.
Top product codes for Wontech Co., Ltd.
Recent clearances by Wontech Co., Ltd.
- K252877 — SANDRO Dual
- K250165 — Pastelle
- K251288 — Veincare
- K251094 — Alma Veil
- K243957 — PICOALEX
- K241527 — Pastelle Pro
- K241643 — WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R)
- K243929 — Oligio X
- K241930 — Veincare
- K241406 — Lavieen
- K241144 — Picosecond Nd:YAG Laser (PICOCAREMAJESTY)
- K234104 — PICOANDY (Q-Switched Nd:YAG Laser)
- K240313 — Oligio X
- K240064 — Hair Boom Air / Ulike Hair UpUp / Hair Boom 69 / Hair Boom
- K232106 — Air Gap Fiber
- K223727 — Lavieen
- K231054 — V-Laser
- K223862 — Hair Boom 69, Hair BoomAir, Hair Boom, Ulike Hair UpUp
- K221989 — The Oligio
- K221427 — V-Laser
- K212127 — Picocaremajesty
- K201406 — Picowon
- K200110 — SANDRO Dual
- K192425 — Hair Boom 69, Hair Boom Air, Ulike Hair UpUp
- K183563 — Holinwon 30
- K183156 — V-Laser
- K181272 — Picocare Family
- K162755 — Picocare
Data sourced from openFDA. This site is unofficial and independent of the FDA.