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Medpac

Country not established

Devices
3

What Medpac makes

Medpac manufactures orthopedic fixation devices, including the Hawaiian Supracondylar Plate for elbow stabilization and Small Fragment Plates and Screws for fracture fixation. The company also produces the SFC, a specialized fixation system for bone stabilization.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Medpac operates from the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Hawaiian Supracondylar Plate Ref K903697

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Sfc Ref K951303

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Small Fragment Plates And Screws Ref K951302

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

Frequently asked questions

How many devices does Medpac have in the registry?

The registry currently lists 3 devices for Medpac. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medpac's devices?

Among its 3 most recently registered devices, Medpac has devices listed in FDA 510(k) (3 devices).

What risk classes do Medpac's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Medpac's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medpac in the registry?

The most recently registered devices listed for Medpac include HAWAIIAN SUPRACONDYLAR PLATE, SFC and SMALL FRAGMENT PLATES AND SCREWS.

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