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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.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Theraform Standard/Sheet Ref K090812

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Theraform Bilayer Ref K090823

    Active Regimes: 510(k) Registry: 510(k) Class:—

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.

Generated automatically from registry data and not verified by a human reviewer.