Medical Device Manufacturer · US , Santa Fe Springs , CA

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

2 submissions · 2 cleared · Since 2009

Recent clearances: THERAFORM BILAYER, THERAFORM STANDARD/SHEET

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sewon Cellontech Co., Ltd. General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Oct 22, 2009

THERAFORM BILAYER

General & Plastic Surgery · 210d

Cleared Jul 30, 2009

THERAFORM STANDARD/SHEET

General & Plastic Surgery · 127d