Maillefer Instruments S.A.
Country not established
- Devices
- 1
What Maillefer Instruments S.A. makes
Maillefer Instruments S.A. manufactures orthopedic surgical tools, including kits designed for cement removal and bone preparation during procedures. These products are intended for use in joint replacement surgeries to facilitate precise bone manipulation and debris clearance.
The company’s portfolio is regulated under FDA’s 510(k) pathway as Class I medical devices, indicating low to moderate risk. These devices are listed in the FDA’s 510(k) clearance registry, and the manufacturer operates from the United States.
Catalogue
Cement And Bone Removal Kit Ref K961759
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maillefer Instruments S.A. have in the registry?
The registry currently lists 1 device for Maillefer Instruments S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maillefer Instruments S.A.'s devices?
Among its 1 most recently registered device, Maillefer Instruments S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Maillefer Instruments S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maillefer Instruments S.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Maillefer Instruments S.A. in the registry?
The most recently registered devices listed for Maillefer Instruments S.A. include CEMENT AND BONE REMOVAL KIT.