Medical Device Manufacturer · KR , Daejeon

Wontech Co., Ltd. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 2017
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) Regulatory Record - Wontech Co., Ltd.
28 devices
1-12 of 28
Cleared Dec 19, 2025
SANDRO Dual
K252877 · GEX
General & Plastic Surgery · 100d
Cleared Jul 03, 2025
Pastelle
K250165 · GEX
General & Plastic Surgery · 163d
Cleared May 14, 2025
Veincare
K251288 · GEX
General & Plastic Surgery · 19d
Cleared May 06, 2025
Alma Veil
K251094 · GEX
General & Plastic Surgery · 26d
Cleared Mar 12, 2025
PICOALEX
K243957 · GEX
General & Plastic Surgery · 79d
Cleared Feb 14, 2025
Pastelle Pro
K241527 · GEX
General & Plastic Surgery · 260d
Cleared Feb 14, 2025
WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R)
K241643 · GEX
General & Plastic Surgery · 252d
Cleared Jan 21, 2025
Oligio X
K243929 · GEI
General & Plastic Surgery · 32d
Cleared Nov 14, 2024
Veincare
K241930 · GEX
General & Plastic Surgery · 136d
Cleared Jun 28, 2024
Lavieen
K241406 · GEX
General & Plastic Surgery · 42d
Cleared Jun 24, 2024
Picosecond Nd:YAG Laser (PICOCAREMAJESTY)
K241144 · GEX
General & Plastic Surgery · 60d
Cleared Mar 15, 2024
PICOANDY (Q-Switched Nd:YAG Laser)
K234104 · GEX
General & Plastic Surgery · 80d
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