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Mtp Solutions, LLC

United StatesFDA applicant, unverified

Devices
4

What Mtp Solutions, LLC makes

Mtp Solutions, LLC manufactures orthopedic implants and fixation devices, including one-piece PEEK fusion implants, titanium suture anchors, and threaded PEEK K-wires. These products are designed for spinal and joint stabilization procedures, providing structural support during surgical interventions.

The company’s portfolio is classified under FDA Class II devices and is listed via the 510(k) premarket notification process. These devices are regulated under U.S. medical device laws and are intended for use within the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

  • One-Piece Peek Fusion Implant Ref K140970

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Titanium Suture Anchor Ref K133229

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Threaded Peek K-Wire Ref K133235

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Peek Fusion Implant Ref K133515

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

Frequently asked questions

How many devices does Mtp Solutions, LLC have in the registry?

The registry currently lists 4 devices for Mtp Solutions, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mtp Solutions, LLC's devices?

Among its 4 most recently registered devices, Mtp Solutions, LLC has devices listed in FDA 510(k) (4 devices).

What risk classes do Mtp Solutions, LLC's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Mtp Solutions, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mtp Solutions, LLC in the registry?

The most recently registered devices listed for Mtp Solutions, LLC include ONE-PIECE PEEK FUSION IMPLANT, TITANIUM SUTURE ANCHOR, THREADED PEEK K-WIRE and PEEK FUSION IMPLANT.

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