Mathys Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Mathys Corp. makes
Mathys Corp. manufactures the CEROS 80, a hip arthroplasty (HA) system designed for total hip replacement procedures. This product includes components intended for primary and revision arthroplasty in the hip joint, providing options for acetabular and femoral replacements.
The CEROS 80 is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ceros Tcp Granules Ref K101426
Regimes: 510(k) Registry: 510(k)Ceros 80 (Ha) Ref K900136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mathys Corp. have in the registry?
The registry currently lists 2 devices for Mathys Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mathys Corp.'s devices?
Among its 2 most recently registered devices, Mathys Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mathys Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mathys Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mathys Corp. in the registry?
The most recently registered devices listed for Mathys Corp. include CEROS TCP GRANULES and CEROS 80 (HA).