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Biomedia, Inc.

United StatesFDA applicant, unverified

Devices
19

What Biomedia, Inc. makes

Biomedia, Inc. manufactures microbiological culture media and related diagnostic products, including various agar plates such as Tryptic Soy Agar with sheep blood, EMB/Mueller-Hinton Agar, Thayer Martin Agar, MacConkey Agar, Chocolate Agar, and Mueller-Hinton Agar poured into plates. The company also produces culture and sensitivity kits and specialized diagnostic systems like the #50002 Quad Diagnostic System and #2010 Campylobacter Agar.

The devices manufactured by Biomedia, Inc. are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

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

Catalogue19

Newest first, rows 1-19 of 19

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  • Strep Blood Agar-5% Sheep Blood Ref K790469

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

  • Dtm (Dermatophyte Test Medium) Agar Ref K791414

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

  • Modified Thayer Martin Agar Ref K790368

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

  • Tryptic Soy Agar W/5% & 10% Sheep Blood Ref K811475

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

  • Emb/Mueller-Hinton Agar Ref K790369

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

  • Thayer Martin Agar Ref K811476

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

  • Bi Plate-Xld/Hektoen #30012 Ref K821108

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

  • Mueller Hinton Agar, Poured Into A Plate Ref K811472

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

  • Culture And Sensitivity Kit Ref K791413

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

  • Mueller Hinton Agar Ref K811471

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

  • Macconkey Agar Ref K811477

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

  • Chodolate Agar, Enriched Ref K811479

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

  • Emb Agar, Levine Ref K811478

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

  • #2010 Camphylobacter Agar Ref K821300

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

  • #50002 Quad Diagnostic System Ref K821301

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

  • #50003 Quad Diagnostic System Ref K821302

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

  • Tryptic Soy Agar W/5% Sheep Blood & Emb Ref K811474

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

  • Bacitracin Differentiation Disc Ref K802127

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

  • Mueller Hinton Agar W/5% Sheep Blood Ref K811473

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

Rows 1-19 of 19

Frequently asked questions

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

The registry currently lists 19 devices for Biomedia, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Biomedia, Inc.'s devices?

Among its 19 most recently registered devices, Biomedia, Inc. has devices listed in FDA 510(k) (19 devices).

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

Among its 19 most recently registered devices, the classes recorded for Biomedia, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Biomedia, Inc. include STREP BLOOD AGAR-5% SHEEP BLOOD, DTM (DERMATOPHYTE TEST MEDIUM) AGAR, MODIFIED THAYER MARTIN AGAR and TRYPTIC SOY AGAR W/5% & 10% SHEEP BLOOD.

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