Dr. Jean-Marc Guichet
Country not established
- Devices
- 1
What Dr. Jean-Marc Guichet makes
Dr. Jean-Marc Guichet manufactures the TITAN Total Hip Device, a prosthetic implant designed for total hip arthroplasty procedures. This product is intended to replace damaged or diseased hip joints, restoring mobility and function in patients.
The TITAN Total Hip Device is classified as a Class II medical device under US regulations and is listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
Titan Total Hip Device Ref K905298
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Jean-Marc Guichet have in the registry?
The registry currently lists 1 device for Dr. Jean-Marc Guichet. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Jean-Marc Guichet's devices?
Among its 1 most recently registered device, Dr. Jean-Marc Guichet has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Jean-Marc Guichet's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Jean-Marc Guichet's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Jean-Marc Guichet in the registry?
The most recently registered devices listed for Dr. Jean-Marc Guichet include TITAN TOTAL HIP DEVICE.