Johnson & Johnson Orthopaedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 22
What Johnson & Johnson Orthopaedics, Inc. makes
Johnson & Johnson Orthopaedics, Inc. manufactures orthopaedic implants for hip and knee replacements, including porous-coated and modular femoral components, acetabular cups, unipolar and total hip systems, patellar components, and ceramic hip heads. Their portfolio also includes knee systems such as unicondylar and total knee implants with modular femoral and tibial components, as well as cemented and uncemented fixation options.
These devices are regulated under FDA Class I and Class II classifications and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Johnson & Johnson Orthopaedics, Inc. have in the registry?
The registry currently lists 22 devices for Johnson & Johnson Orthopaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johnson & Johnson Orthopaedics, Inc.'s devices?
Among its 22 most recently registered devices, Johnson & Johnson Orthopaedics, Inc. has devices listed in FDA 510(k) (22 devices).
What risk classes do Johnson & Johnson Orthopaedics, Inc.'s devices fall under?
Among its 22 most recently registered devices, the classes recorded for Johnson & Johnson Orthopaedics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Johnson & Johnson Orthopaedics, Inc. in the registry?
The most recently registered devices listed for Johnson & Johnson Orthopaedics, Inc. include P.F.C. HIP SYSTEM NON-POROUS ACETABULAR COMPONENT, P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT, ULTIMA UNIPOLAR MODULAR HEAD and INSET PATELLAR COMPONENT.