Wontech Co., Ltd. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Wontech Co., Ltd. has 28 FDA 510(k) cleared general & plastic surgery devices. Based in Daejeon, KR.
Latest FDA clearance: Dec 2025. Active since 2017.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Wontech Co., Ltd.
21 devices
Cleared
Dec 19, 2025
SANDRO Dual
General & Plastic Surgery
100d
Cleared
Jul 03, 2025
Pastelle
General & Plastic Surgery
163d
Cleared
May 14, 2025
Veincare
General & Plastic Surgery
19d
Cleared
May 06, 2025
Alma Veil
General & Plastic Surgery
26d
Cleared
Mar 12, 2025
PICOALEX
General & Plastic Surgery
79d
Cleared
Feb 14, 2025
Pastelle Pro
General & Plastic Surgery
260d
Cleared
Feb 14, 2025
WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R)
General & Plastic Surgery
252d
Cleared
Jan 21, 2025
Oligio X
General & Plastic Surgery
32d
Cleared
Nov 14, 2024
Veincare
General & Plastic Surgery
136d
Cleared
Jun 28, 2024
Lavieen
General & Plastic Surgery
42d
Cleared
Jun 24, 2024
Picosecond Nd:YAG Laser (PICOCAREMAJESTY)
General & Plastic Surgery
60d
Cleared
Mar 15, 2024
PICOANDY (Q-Switched Nd:YAG Laser)
General & Plastic Surgery
80d