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Intermedics Orthopedics

Country not established

Devices
108

What Intermedics Orthopedics makes

Intermedics Orthopedics manufactures orthopedic implants and surgical instruments for joint reconstruction, including femoral and humeral stems for hip and shoulder prostheses, bipolar and unipolar hip prostheses, high tibial osteotomy systems, and fracture fixation stems. Their portfolio also includes modular shoulder components, press-fit hip systems, and knee implants designed for primary and revision arthroplasty procedures.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory clearance status. The manufacturer operates from the United States.

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

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Frequently asked questions

How many devices does Intermedics Orthopedics have in the registry?

The registry currently lists 108 devices for Intermedics Orthopedics. Devices recorded under merged duplicate company entries are counted once.

Which registries list Intermedics Orthopedics's devices?

Among its 50 most recently registered devices, Intermedics Orthopedics has devices listed in FDA 510(k) (50 devices).

What risk classes do Intermedics Orthopedics's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Intermedics Orthopedics's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Intermedics Orthopedics in the registry?

The most recently registered devices listed for Intermedics Orthopedics include DRG CEMETED STEM, INTERMEDICS POWER BROACH IMPACTOR, INTERMEDICS HIGH TIBIAL OSTEOTOMY SYSTEM and IOI BIPOLAR PROSTHESIS.

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