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Suzhou Colour-Way Enterprise Development Co., Ltd.

ChinaFDA applicant, unverified

Devices
2

What Suzhou Colour-Way Enterprise Development Co., Ltd. makes

Suzhou Colour-Way Enterprise Development Co., Ltd. manufactures powdered latex surgeon's gloves and devices under the M. Dior brand.

The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • M. Dior Brand Ref K083817

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Powdered Latex Surgeon's Glove Ref K121925

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

Frequently asked questions

How many devices does Suzhou Colour-Way Enterprise Development Co., Ltd. have in the registry?

The registry currently lists 2 devices for Suzhou Colour-Way Enterprise Development Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Suzhou Colour-Way Enterprise Development Co., Ltd.'s devices?

Among its 2 most recently registered devices, Suzhou Colour-Way Enterprise Development Co., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Suzhou Colour-Way Enterprise Development Co., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Suzhou Colour-Way Enterprise Development Co., Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Suzhou Colour-Way Enterprise Development Co., Ltd. in the registry?

The most recently registered devices listed for Suzhou Colour-Way Enterprise Development Co., Ltd. include M. DIOR BRAND and POWDERED LATEX SURGEON'S GLOVE.

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