Excera Orthopedics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Excera Orthopedics, Inc. makes
Excera Orthopedics, Inc. manufactures the FitRite™ Total Hip Arthroplasty System, a Class II medical device designed for total hip replacement procedures. This system includes components intended for use in arthroplasty surgeries to restore hip joint function in patients with degenerative joint disease or trauma.
The company’s portfolio is regulated under the FDA’s 510(k) pathway as Class II devices. The FitRite™ Total Hip Arthroplasty System is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Excera Fitrite Total Hip Arthroplasty System Ref K140547
510(k) 510(k)FitRite™ Total Hip Arthroplasty System Ref K153057
510(k) 510(k)
Frequently asked questions
How many devices does Excera Orthopedics, Inc. have in the registry?
The registry currently lists 2 devices for Excera Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Excera Orthopedics, Inc.'s devices?
Among its 2 most recently registered devices, Excera Orthopedics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Excera Orthopedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Excera Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Excera Orthopedics, Inc. in the registry?
The most recently registered devices listed for Excera Orthopedics, Inc. include EXCERA FITRITE TOTAL HIP ARTHROPLASTY SYSTEM and FitRite™ Total Hip Arthroplasty System.