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Proasia Limited

Country not established

Devices
3

What Proasia Limited makes

Proasia Limited manufactures patient examination gloves, including models L4501 and L3402, designed for clinical use.

These products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Patient Examination Gloves Ref K893632

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Proasia, Model L4501 Ref K052486

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Proasia, Model L3402 Ref K052378

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

Frequently asked questions

How many devices does Proasia Limited have in the registry?

The registry currently lists 3 devices for Proasia Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list Proasia Limited's devices?

Among its 3 most recently registered devices, Proasia Limited has devices listed in FDA 510(k) (3 devices).

What risk classes do Proasia Limited's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Proasia Limited's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Proasia Limited in the registry?

The most recently registered devices listed for Proasia Limited include PATIENT EXAMINATION GLOVES, PROASIA, MODEL L4501 and PROASIA, MODEL L3402.

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