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Tissue Technologies, Inc.

United StatesFDA applicant, unverified

Devices
9

What Tissue Technologies, Inc. makes

Tissue Technologies, Inc. manufactures soft tissue augmentation devices, including tubes and implants for facial augmentation, as well as CO₂ surgical lasers for tissue resurfacing and modification. Products include the YUBE with insertion tool, S.T.A.T. tubes, SoftForm facial implants, and Tru-Pulse CO₂ laser systems designed for dermatological and reconstructive procedures.

The company’s portfolio consists of Class II medical devices, all of which are authorised via FDA 510(k) clearance. These devices are listed under the FDA’s regulatory framework and are intended for use in the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

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

The registry currently lists 9 devices for Tissue Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tissue Technologies, Inc.'s devices?

Among its 9 most recently registered devices, Tissue Technologies, Inc. has devices listed in FDA 510(k) (9 devices).

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

Among its 9 most recently registered devices, the classes recorded for Tissue Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Tissue Technologies, Inc. include SOFT TISSUE AUGMENTATION YUBE WITH INSERTION TOOL, SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.), SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLES and SOFTFORM FACIAL IMPLANT.

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