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Princeton Medical Instruments, Inc.

United StatesFDA applicant, unverified

Devices
2

What Princeton Medical Instruments, Inc. makes

Princeton Medical Instruments, Inc. manufactures syringe infusion pumps and syringe drivers, including the MS 16 Syringe Driver, designed for controlled medication delivery in clinical settings.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Syringe Infusion Pump Ref K791729

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ms 16 Syringe Driver Ref K802400

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

Frequently asked questions

How many devices does Princeton Medical Instruments, Inc. have in the registry?

The registry currently lists 2 devices for Princeton Medical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Princeton Medical Instruments, Inc.'s devices?

Among its 2 most recently registered devices, Princeton Medical Instruments, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Princeton Medical Instruments, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Princeton Medical Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Princeton Medical Instruments, Inc. in the registry?

The most recently registered devices listed for Princeton Medical Instruments, Inc. include SYRINGE INFUSION PUMP and MS 16 SYRINGE DRIVER.

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