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Robert Bosch Corp.

United StatesFDA applicant, unverified

Devices
21

What Robert Bosch Corp. makes

Robert Bosch Corp. manufactures hearing aids such as post-auricular and in-the-ear models including the STAR 33PP, 44, 55F, Superstar, STAR 66F-AGC-I, and STAR 66PP-S, as well as hearing aid analysis systems. The company also produces ergometer bicycles (ERG 550, ERG 551), impedance cardiography devices (IMPULS 3, IT SELECTOR), defibrillators (DEFI 502), electrocardiogram systems (ECS 502), ultrasound systems (ULTRAMED 11S601), and vacuum-assisted wound therapy devices (VACOMED 4).

These devices 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.

Catalogue21

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  • Impuls 3, It Selector Ref K842805

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

  • Post Auricular Hearing Aids Star 33PP, 44, 55F & Ref K850186

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

  • Defi 502 Ref K851485

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

  • Bosch In The Ear Hearing Aid Superstar Ref K850188

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

  • Erg 550 Ergometer Bicycle Ref K854491

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

  • Hearing Aid Analysis System Ref K853271

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

  • Vacomed 4 Ref K842802

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

  • Erg 551 Ergometer, Bicycle Ref K854492

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

  • Star 66F-Agc-I Hearing Aid Ref K850190

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

  • Ecs 502 Ref K840717

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

  • Ultramed 11S601 Ref K842801

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

  • Bosch Star 66PP-S Hearing Aid Ref K850189

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

  • Bosch Starr 66PP -Hearing Aids Ref K850187

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

  • Hv-4 Ref K853154

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

  • Tonotest Blood Pressure Device Ref K790682

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

  • Sonomed 4 Ref K851937

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

  • Sp 4 Ref K853541

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

  • Erg 555 Couch Ergometer Ref K854493

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

  • Interferenz 4 Ref K842803

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

  • Body Hearing Aids Mt 80 Sp Ref K850185

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

  • Diadyn 4 Ref K842804

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

Rows 1-21 of 21

Frequently asked questions

How many devices does Robert Bosch Corp. have in the registry?

The registry currently lists 21 devices for Robert Bosch Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Robert Bosch Corp.'s devices?

Among its 21 most recently registered devices, Robert Bosch Corp. has devices listed in FDA 510(k) (21 devices).

What risk classes do Robert Bosch Corp.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Robert Bosch Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Robert Bosch Corp. in the registry?

The most recently registered devices listed for Robert Bosch Corp. include IMPULS 3, IT SELECTOR, POST AURICULAR HEARING AIDS STAR 33PP, 44, 55F &, DEFI 502 and BOSCH IN THE EAR HEARING AID SUPERSTAR.

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