Skip to content

Soft Tissue Regeneration, Inc.

Country not established

Devices
1

What Soft Tissue Regeneration, Inc. makes

Soft Tissue Regeneration, Inc. produces the STR GRAFT, a Class II medical device used for soft tissue regeneration.

The company is based in the US, and its devices are listed in the FDA 510(k) registry, which regulates Class II medical devices.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Str Graft Ref K121216

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

Frequently asked questions

How many devices does Soft Tissue Regeneration, Inc. have in the registry?

The registry currently lists 1 device for Soft Tissue Regeneration, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Soft Tissue Regeneration, Inc.'s devices?

Among its 1 most recently registered device, Soft Tissue Regeneration, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Soft Tissue Regeneration, Inc.'s devices fall under?

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

What are the newest devices from Soft Tissue Regeneration, Inc. in the registry?

The most recently registered devices listed for Soft Tissue Regeneration, Inc. include STR GRAFT.

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