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Tissue Technologies Holdings, LLC

United StatesFDA applicant, unverified

Devices
2

What Tissue Technologies Holdings, LLC makes

Tissue Technologies Holdings, LLC manufactures the TT101 series (models TT 101-1 through -8) and the TT-102, which are classified as Class U (Custom Device) medical devices under FDA regulations.

These devices are listed in the FDA’s 510(k) registry and are regulated as custom devices, requiring premarket submission for compliance. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • TT101, Models Tt 101-1, -2, -3, -4, -5, -6, -7, -8 Ref K061060

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

  • Tt-102 Ref K081246

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

Frequently asked questions

How many devices does Tissue Technologies Holdings, LLC have in the registry?

The registry currently lists 2 devices for Tissue Technologies Holdings, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tissue Technologies Holdings, LLC's devices?

Among its 2 most recently registered devices, Tissue Technologies Holdings, LLC has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Tissue Technologies Holdings, LLC in the registry?

The most recently registered devices listed for Tissue Technologies Holdings, LLC include TT101, MODELS TT 101-1, -2, -3, -4, -5, -6, -7, -8 and TT-102.

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