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Pharma-Plast USA, Inc.

Country not established

Devices
9

What Pharma-Plast USA, Inc. makes

Pharma-Plast USA, Inc. manufactures single-use medical devices including intravenous and insulin infusion sets, needle-based products (such as blood drawing and dental needles), tracheal tubes, and safety-engineered needles and holders. Their portfolio also covers syringe systems, including pre-filled and single-use options, as well as catheter products designed for medical and dental applications.

The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. These items are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

  • Pharma-Plast Clinipak Ref K852443

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Pharma-Plast Needle Ref K852442

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Asik 'once' Syringe Ref K852444

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nipro Safelet Cath Ref K894371

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Pharma-Plast Insulin Infusion Set Ref K884978

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nipro Needle Holder Ref K894372

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Blood Drawing Needle Ref K894374

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Multiple Pharma-Plast Tracheal Tube Ref K871263

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nipro Dental Needle Ref K894373

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

Frequently asked questions

How many devices does Pharma-Plast USA, Inc. have in the registry?

The registry currently lists 9 devices for Pharma-Plast USA, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pharma-Plast USA, Inc.'s devices?

Among its 9 most recently registered devices, Pharma-Plast USA, Inc. has devices listed in FDA 510(k) (9 devices).

What risk classes do Pharma-Plast USA, Inc.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Pharma-Plast USA, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pharma-Plast USA, Inc. in the registry?

The most recently registered devices listed for Pharma-Plast USA, Inc. include PHARMA-PLAST CLINIPAK, PHARMA-PLAST NEEDLE, ASIK 'ONCE' SYRINGE and NIPRO SAFELET CATH.

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