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Jj Implants

IndiaFDA applicant, unverified

Devices
1

What Jj Implants makes

Jj Implants manufactures the JJ Implant System, a medical device designed for internal use in orthopedic applications, likely for joint stabilization or reconstruction.

The device falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • JJ Implant System Ref K190552

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

Frequently asked questions

How many devices does Jj Implants have in the registry?

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

Which registries list Jj Implants's devices?

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

What risk classes do Jj Implants's devices fall under?

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

What are the newest devices from Jj Implants in the registry?

The most recently registered devices listed for Jj Implants include JJ Implant System.

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