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Verimed Holdings, Inc.

United StatesFDA applicant, unverified

Devices
12

What Verimed Holdings, Inc. makes

Verimed Holdings, Inc. manufactures electro-myographic devices for muscle assessment and stimulation, including perineometers for pelvic floor function evaluation, myo-exercisers for muscle activation training, and biofeedback systems for real-time physiological monitoring. Their portfolio also includes range-of-motion assessment tools and actuated devices designed to support neuromuscular rehabilitation and functional testing.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance database. Products are listed under U.S. jurisdiction, adhering to applicable medical device regulations.

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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  • Verimed Myoexorciser Ref K832714

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

  • Phyaction 787 Ref K930670

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

  • Verimed Myo/Prems Ref K874212

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

  • Myo-Actuator Ref K852963

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

  • Biofeedback Device Ref K954127

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

  • Verimed Myoexorciser Veristim Ref K893220

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

  • Verimed Myoexorciser Iii (Myo Iii) Ref K892649

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

  • Myoexorciser Ii Fual Ref K951969

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

  • Electro-Myographic Perineometer Ref K854193

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

  • Periform Ref K981277

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

  • Romas (Range Of Motion Assessment System) Ref K922550

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

  • Verimed Perineometer Ref K913912

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

Rows 1-12 of 12

Frequently asked questions

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

The registry currently lists 12 devices for Verimed Holdings, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Verimed Holdings, Inc.'s devices?

Among its 12 most recently registered devices, Verimed Holdings, Inc. has devices listed in FDA 510(k) (12 devices).

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

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

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

The most recently registered devices listed for Verimed Holdings, Inc. include VERIMED MYOEXORCISER, PHYACTION 787, VERIMED MYO/PREMS and MYO-ACTUATOR.

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