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Medi-Plast Intl., Inc.

United StatesFDA applicant, unverified

Devices
12

What Medi-Plast Intl., Inc. makes

Medi-Plast Intl., Inc. manufactures medical devices including syringes, compression dressings, IV bottles and bags, glass vials, fluoroscope band bags, operating room and heart catheterization tray sets, sterile pan sets, and disposable manifolds such as the Medi-Plast 2 Port Manifold and bottle-to-bottle systems.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Medi-Plast Intl., Inc. is based in the United States.

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

Catalogue12

Newest first, rows 1-12 of 12

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  • 10cc Control Syringe Ref K873588

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

  • Arterial-Venous Compression Dressing Ref K851489

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

  • I.V. Bottle (Ridgid) Ref K811234 Open recall

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

  • Glass Vials Ref K811269 Open recall

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

  • Fluoroscope Band Bag Ref K861785

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

  • Operating Room Tray Set Ref K840021

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

  • Heart Catheterization Tray Set Ref K840022

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

  • I.V. Plastic Bag Ref K811233 Open recall

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

  • Sterile Pan Set Ref K842136

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

  • Medi-Plast Disposable Manifold Ref K863402

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

  • Bottle-To-Bottle Ref K811268 Open recall

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

  • Medi-Plast 2 Port Manifold (Right On) Ref K954284

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

Rows 1-12 of 12

Frequently asked questions

How many devices does Medi-Plast Intl., Inc. have in the registry?

The registry currently lists 12 devices for Medi-Plast Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medi-Plast Intl., Inc.'s devices?

Among its 12 most recently registered devices, Medi-Plast Intl., Inc. has devices listed in FDA 510(k) (12 devices).

What risk classes do Medi-Plast Intl., Inc.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Medi-Plast Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medi-Plast Intl., Inc. in the registry?

The most recently registered devices listed for Medi-Plast Intl., Inc. include 10CC CONTROL SYRINGE, ARTERIAL-VENOUS COMPRESSION DRESSING, I.V. BOTTLE (RIDGID) and GLASS VIALS.

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