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Implantology Corp.

United StatesFDA applicant, unverified

Devices
9

What Implantology Corp. makes

Implantology Corp. manufactures orthopedic implants for hip and knee replacements, including femoral stem components, acetabular components, bipolar femoral heads, and total knee systems. Their portfolio includes resurfacing knees, posterior-stabilized knee prostheses, and hydroxyapatite-coated hip stems designed for primary and revision surgeries.

The company’s devices are classified as Class II and Class III under FDA regulations, with submissions recorded in the 510(k) clearance pathway. These products are intended for use in the United States, where they are subject to FDA oversight.

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

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Implantology Corp. have in the registry?

The registry currently lists 9 devices for Implantology Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Implantology Corp.'s devices?

Among its 9 most recently registered devices, Implantology Corp. has devices listed in FDA 510(k) (9 devices).

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

Among its 9 most recently registered devices, the classes recorded for Implantology Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Implantology Corp. in the registry?

The most recently registered devices listed for Implantology Corp. include UFC HIP STEM COMPONENT, PSK POSTERIOR STABILIZED TOATAL KNEE, FPC/SFPC/RFPC ACETABULAR COMPONENT and PPC HIP STEM COMPONENT.

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