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Medivices Co.

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Devices
1

What Medivices Co. makes

Medivices Co. manufactures hernia mesh stabilizers, which are surgical implants designed to reinforce abdominal wall repairs and prevent hernia recurrence by securing mesh in place during reconstructive procedures.

These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Hernia Mesh Stabilizer Ref K981598

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

Frequently asked questions

How many devices does Medivices Co. have in the registry?

The registry currently lists 1 device for Medivices Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medivices Co.'s devices?

Among its 1 most recently registered device, Medivices Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Medivices Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Medivices Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medivices Co. in the registry?

The most recently registered devices listed for Medivices Co. include HERNIA MESH STABILIZER.

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