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Dow Corning Wright

Country not established

Devices
75

What Dow Corning Wright makes

Dow Corning Wright manufactures orthopedic implants and medical devices for joint replacement, including femoral hip stems, knee prostheses, tibial and femoral revision components, and patellar implants. Their portfolio also includes silicone-based soft sheeting for medical applications and vascular catheters for hemodialysis. The company produces posterior-stabilized knee systems and metal-backed patella components.

The company’s devices are regulated under FDA classifications including Class I, Class II, Class III, and Unclassified (U), with some authorised via 510(k) clearance and others through PMA approval. Their products are listed in the FDA’s regulatory databases for medical devices, and the company is headquartered in 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 Dow Corning Wright have in the registry?

The registry currently lists 75 devices for Dow Corning Wright. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dow Corning Wright's devices?

Among its 50 most recently registered devices, Dow Corning Wright has devices listed in FDA 510(k) (50 devices).

What risk classes do Dow Corning Wright's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Dow Corning Wright'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 Dow Corning Wright in the registry?

The most recently registered devices listed for Dow Corning Wright include SILASTIC SOFT SHEETING, NEXUS(TM) FEMORAL HIP STEM, ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT and ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT.

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