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Impex Laboratories

Country not established

Devices
3

What Impex Laboratories makes

Impex Laboratories manufactures hypodermic needles, which are classified as Class II medical devices.

These devices are regulated under the FDA 510(k) pathway and the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Syringes(2-Parts Single Use) Ref K822532

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Syringes(3-Parts Single Use) Ref K822533

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Needles(Hypodermic) Ref K822534

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

Frequently asked questions

How many devices does Impex Laboratories have in the registry?

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

Which registries list Impex Laboratories's devices?

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

What risk classes do Impex Laboratories's devices fall under?

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

What are the newest devices from Impex Laboratories in the registry?

The most recently registered devices listed for Impex Laboratories include SYRINGES(2-PARTS SINGLE USE), SYRINGES(3-PARTS SINGLE USE) and NEEDLES(HYPODERMIC).

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