Sulzer Orthopedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 45
What Sulzer Orthopedics, Inc. makes
The company manufactures orthopedic joint replacement components, including hip and knee prostheses such as porous-coated stems, acetabular systems, tibial inserts, femoral spacers, and revision stems. Products include modular hip systems with offset stems, posterior-stabilized knee inserts, uniconylar spacers, and patellofemoral joint prostheses designed for primary and revision surgeries.
These devices are regulated under FDA 510(k) clearance, with classifications spanning Class II and Class III. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Search and filter all 45 devicesFrequently asked questions
How many devices does Sulzer Orthopedics, Inc. have in the registry?
The registry currently lists 45 devices for Sulzer Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sulzer Orthopedics, Inc.'s devices?
Among its 45 most recently registered devices, Sulzer Orthopedics, Inc. has devices listed in FDA 510(k) (45 devices).
What risk classes do Sulzer Orthopedics, Inc.'s devices fall under?
Among its 45 most recently registered devices, the classes recorded for Sulzer Orthopedics, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Sulzer Orthopedics, Inc. in the registry?
The most recently registered devices listed for Sulzer Orthopedics, Inc. include NATURAL-HIP COCR OFFSET STEM, SULZER ORTHOPEDICS CONVERGE ACETABULAR SYSTEM, NATURAL-KNEE II POSTERIOR STABILIZED (P.S.) CONDYLAR KNEE TIBIAL INSERTS and NATURAL-HIP POROUS STEM WITH OFFSET.