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Techmedica, Inc.

United StatesFDA applicant, unverified

Devices
31

What Techmedica, Inc. makes

Techmedica, Inc. manufactures orthopedic implants and surgical instruments, including cemented and bipolar hip systems, knee prostheses (unicompartmental and total), femoral stems, patella replacements, bone staples, and specialized blades for bone preparation. Their portfolio also includes modular hip systems, osteotomy tools like the hole chamfering device, and instruments for knee arthroplasty.

The company’s devices are regulated under the FDA’s 510(k) pathway and span Class I, Class II, and Class III classifications. Products are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Techmedica, Inc. have in the registry?

The registry currently lists 31 devices for Techmedica, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Techmedica, Inc.'s devices?

Among its 31 most recently registered devices, Techmedica, Inc. has devices listed in FDA 510(k) (31 devices).

What risk classes do Techmedica, Inc.'s devices fall under?

Among its 31 most recently registered devices, the classes recorded for Techmedica, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Techmedica, Inc. in the registry?

The most recently registered devices listed for Techmedica, Inc. include TECHMEDICA STANDARD CEMENTED HIP SYSTEM, CONTINUUM KNEE SYSTEM (CKS), CKS OSCILLATING SAW BLADE and TECHMEDIA BONE STAPLE.

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