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Wuhrlin Soplamed (M) Sdn Bhd

MalaysiaFDA applicant, unverified

Devices
2

What Wuhrlin Soplamed (M) Sdn Bhd makes

Wuhrlin Soplamed (M) Sdn Bhd manufactures patient examination gloves and surgeon’s gloves, designed for sterile and non-sterile use in clinical settings.

These products fall under Class I medical devices and are listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Patient Examination Gloves Ref K924386

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgeon's Glove Ref K925030

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

Frequently asked questions

How many devices does Wuhrlin Soplamed (M) Sdn Bhd have in the registry?

The registry currently lists 2 devices for Wuhrlin Soplamed (M) Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.

Which registries list Wuhrlin Soplamed (M) Sdn Bhd's devices?

Among its 2 most recently registered devices, Wuhrlin Soplamed (M) Sdn Bhd has devices listed in FDA 510(k) (2 devices).

What risk classes do Wuhrlin Soplamed (M) Sdn Bhd's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Wuhrlin Soplamed (M) Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Wuhrlin Soplamed (M) Sdn Bhd in the registry?

The most recently registered devices listed for Wuhrlin Soplamed (M) Sdn Bhd include PATIENT EXAMINATION GLOVES and SURGEON'S GLOVE.

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