Sewon Cellontech Co., Ltd.
Country not established
- Devices
- 2
What Sewon Cellontech Co., Ltd. makes
Sewon Cellontech Co., Ltd. manufactures THERAFORM STANDARD/SHEET and THERAFORM BILAYER, which are wound dressings used for medical purposes.
These devices are classified as Class U and are listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Theraform Standard/Sheet Ref K090812
Regimes: 510(k) Registry: 510(k)Theraform Bilayer Ref K090823
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sewon Cellontech Co., Ltd. have in the registry?
The registry currently lists 2 devices for Sewon Cellontech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sewon Cellontech Co., Ltd.'s devices?
Among its 2 most recently registered devices, Sewon Cellontech Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Sewon Cellontech Co., Ltd. in the registry?
The most recently registered devices listed for Sewon Cellontech Co., Ltd. include THERAFORM STANDARD/SHEET and THERAFORM BILAYER.