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Solidence Surgical Corporation

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Devices
1

What Solidence Surgical Corporation makes

Solidence Surgical Corporation manufactures the Solidence Multipockets, a device designed for surgical applications requiring controlled pocket creation within tissue, likely for hernia repair or soft tissue reinforcement.

The company’s portfolio is regulated under Class II medical devices in the US, with the Solidence Multipockets authorised via the FDA’s 510(k) pathway. The device is listed in the FDA’s 510(k) registry.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Solidence Multipockets Ref K191131

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

Frequently asked questions

How many devices does Solidence Surgical Corporation have in the registry?

The registry currently lists 1 device for Solidence Surgical Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list Solidence Surgical Corporation's devices?

Among its 1 most recently registered device, Solidence Surgical Corporation has devices listed in FDA 510(k) (1 device).

What risk classes do Solidence Surgical Corporation's devices fall under?

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

What are the newest devices from Solidence Surgical Corporation in the registry?

The most recently registered devices listed for Solidence Surgical Corporation include Solidence Multipockets.

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