Maxxos Medical GmbH
GermanyFDA applicant, unverified FDA
- Devices
- 79
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Maxxos Medical GmbH makes
Maxxos Medical GmbH manufactures the MAXXOS P.A.C.E. Foot & Ankle Plating System, a surgical orthopedic device designed for internal fixation of fractures in the foot and ankle.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Search and filter all 79 devicesShowing 1-50 of 79
Company details
- DUNS number
- 313262497
- [email protected]
- Phone
- +4915141807283
FDA establishments
- Maxxos-Medical GmbH Mahlstetten Baden-Wurttemberg · DE FEI 3011354099
Frequently asked questions
How many devices does Maxxos Medical GmbH have in the registry?
The registry currently lists 79 devices for Maxxos Medical GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxxos Medical GmbH's devices?
Among its 50 most recently registered devices, Maxxos Medical GmbH has devices listed in FDA GUDID (50 devices).
What risk classes do Maxxos Medical GmbH's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Maxxos Medical GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxxos Medical GmbH in the registry?
The most recently registered devices listed for Maxxos Medical GmbH include P.A.C.E. M113128-008, P.A.C.E. M113128-010, P.A.C.E. M113128-012 and P.A.C.E. M113128-016.
Which FDA establishments are linked to Maxxos Medical GmbH?
1 FDA establishment is linked to Maxxos Medical GmbH in the registry; they are listed on the company page.