Skip to content

Ballert Orthopedic Corp.

United StatesFDA applicant, unverified

Devices
2

What Ballert Orthopedic Corp. makes

Ballert Orthopedic Corp. manufactures the VERTETRAC, a spinal fixation device designed for internal stabilization, and the EQUALIZER, a modular orthopedic implant used in limb alignment and load distribution procedures.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) premarket notification process. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Vertetrac Ref K771988

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

  • Equalizer Ref K780617

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

Frequently asked questions

How many devices does Ballert Orthopedic Corp. have in the registry?

The registry currently lists 2 devices for Ballert Orthopedic Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ballert Orthopedic Corp.'s devices?

Among its 2 most recently registered devices, Ballert Orthopedic Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Ballert Orthopedic Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Ballert Orthopedic Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Ballert Orthopedic Corp. in the registry?

The most recently registered devices listed for Ballert Orthopedic Corp. include VERTETRAC and EQUALIZER.

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