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Ormed Mfg., Inc.

United StatesFDA applicant, unverified

Devices
23

What Ormed Mfg., Inc. makes

Ormed Mfg., Inc. produces surgical and medical sponges, including blunt sponges, strung neuro sponge patties (X-ray opaque), cylindrical sponges, gauze sponges, and tracheotomy sponges. Their portfolio also includes dissectors like rosebud and modified round (beehive) types, flat stick sponges, and color-coded pre-washed lap sponges. Additionally, they manufacture sterile suture removal sets for post-operative care.

These devices are classified under FDA Class I and Class II (Unclassified), with most listed via the 510(k) pathway. The company’s products are registered in the FDA’s 510(k) database, adhering to U.S. regulatory requirements. Ormed Mfg., Inc. is based in the United States.

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

Catalogue23

Newest first, rows 1-23 of 23

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  • Blunt Sponge Ref K880911

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

  • Strung Neuro Sponge Patties, X-Ray Opague Ref K852202

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

  • Cylindrical Sponge Ref K882528

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

  • Gauze Sponge Ref K882527

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

  • Tracheotomy Sponges Ref K880909

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

  • Rosebud Dissectors Ref K880852

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

  • Flat Stick Sponge Ref K880851

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

  • Modified Round (Beehive) Dissector 3/8 Ref K873391

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

  • Round-Beehive- Dissectors 3/8 Ref K831912

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

  • Color-Eze Pre-Washed Lap Sponges Ref K831913

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

  • Strung Neuro Sponge Patties-X-Ray- Ref K831914

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

  • Sterile Suture Removal Set Ref K832047

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

  • Pre-Rolled Tubular Stockinette Ref K831936

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

  • Ear And Eye Sponges Ref K873831

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

  • Artromot K2 Cpm Ref K931555

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

  • Triangle Sponge Ref K880907

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

  • Strung Absorbent Balls Ref K880854

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

  • Cherry Sponge Ref K880853

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

  • Tape Strung Tonsil Sponge Ref K882530

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

  • Round Stick Sponges Ref K880910

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

  • Safety Pins & Rubber Bands Ref K831915

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

  • Butcher Strung Tonsil Sponge Ref K882529

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

  • Disposable Floor Instruments Ref K831911

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

Rows 1-23 of 23

Frequently asked questions

How many devices does Ormed Mfg., Inc. have in the registry?

The registry currently lists 23 devices for Ormed Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ormed Mfg., Inc.'s devices?

Among its 23 most recently registered devices, Ormed Mfg., Inc. has devices listed in FDA 510(k) (23 devices).

What risk classes do Ormed Mfg., Inc.'s devices fall under?

Among its 23 most recently registered devices, the classes recorded for Ormed Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Ormed Mfg., Inc. in the registry?

The most recently registered devices listed for Ormed Mfg., Inc. include BLUNT SPONGE, STRUNG NEURO SPONGE PATTIES, X-RAY OPAGUE, CYLINDRICAL SPONGE and GAUZE SPONGE.

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