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Implant Technology, Inc.

United StatesFDA applicant, unverified

Devices
13

What Implant Technology, Inc. makes

Implant Technology, Inc. manufactures orthopedic and airway medical devices, including cemented and hydroxyapatite-coated femoral hip implants, total hip systems with Muller-type acetabular cups, and semi-constrained hip joint prostheses. Their portfolio also includes bone cement extractors and tracheostomy tubes, such as the Communi-Trach and related tracheal tubes.

The company’s devices are classified under FDA Class II and are subject to 510(k) clearance in the United States. These products are listed in the FDA’s 510(k) registry, adhering to regulatory requirements for orthopedic and airway medical devices. The manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

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

The registry currently lists 13 devices for Implant Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Implant Technology, Inc.'s devices?

Among its 13 most recently registered devices, Implant Technology, Inc. has devices listed in FDA 510(k) (13 devices).

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

Among its 13 most recently registered devices, the classes recorded for Implant Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Implant Technology, Inc. include LSF HA COATED FEMORAL HIP, LSF CEMENTED FEMORAL HIP, COMMUNITRACH TUBE and IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR.

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