Medicim NV
Country not established
- Devices
- 1
What Medicim NV makes
Medicim NV manufactures MAXILIM, a medical device designed for maxillofacial applications, including orthognathic surgery and dental implants. The product is intended to assist in the stabilization and fixation of bone segments in the jaw, aiding in the alignment and reconstruction of facial structures.
MAXILIM is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States, where its devices are subject to FDA oversight and compliance requirements.
Catalogue
Maxilim Ref K052424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medicim NV have in the registry?
The registry currently lists 1 device for Medicim NV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicim NV's devices?
Among its 1 most recently registered device, Medicim NV has devices listed in FDA 510(k) (1 device).
What risk classes do Medicim NV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medicim NV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicim NV in the registry?
The most recently registered devices listed for Medicim NV include MAXILIM.