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Valpo Orthopedic Technology, Inc.

United StatesFDA applicant, unverified

Devices
2

What Valpo Orthopedic Technology, Inc. makes

Valpo Orthopedic Technology, Inc. manufactures ADJUST-RIGHT FIXATION DEVICES for orthopedic stabilization and UNICOMPARTMENTAL KNEE implants designed for partial knee replacement procedures.

The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. The manufacturer 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

  • Adjust-Right Fixation Devices Ref K062734

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Unicompartmental Knee Ref K072704

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

Frequently asked questions

How many devices does Valpo Orthopedic Technology, Inc. have in the registry?

The registry currently lists 2 devices for Valpo Orthopedic Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Valpo Orthopedic Technology, Inc.'s devices?

Among its 2 most recently registered devices, Valpo Orthopedic Technology, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Valpo Orthopedic Technology, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Valpo Orthopedic Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Valpo Orthopedic Technology, Inc. in the registry?

The most recently registered devices listed for Valpo Orthopedic Technology, Inc. include ADJUST-RIGHT FIXATION DEVICES and UNICOMPARTMENTAL KNEE.

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