Procordia Oratech AB
SwedenFDA applicant, unverified
- Devices
- 1
What Procordia Oratech AB makes
Procordia Oratech AB manufactures the GUIDOR™, a medical device designed for guiding and stabilizing procedures in orthopedic surgery, particularly for hip replacements or related interventions.
The GUIDOR™ 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.
Catalogue
Guidor(Tm) Ref K912724
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Procordia Oratech AB have in the registry?
The registry currently lists 1 device for Procordia Oratech AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Procordia Oratech AB's devices?
Among its 1 most recently registered device, Procordia Oratech AB has devices listed in FDA 510(k) (1 device).
What risk classes do Procordia Oratech AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Procordia Oratech AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Procordia Oratech AB in the registry?
The most recently registered devices listed for Procordia Oratech AB include GUIDOR(TM).