Geyser S.A.
FranceFDA applicant, unverified
- Devices
- 1
What Geyser S.A. makes
Geyser S.A. manufactures the ENDOBOY, a medical device designed for endoscopic procedures, likely used in minimally invasive surgeries or diagnostic imaging within the gastrointestinal or biliary tract.
The ENDOBOY falls under FDA Class II regulation and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Endoboy Ref K033644
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geyser S.A. have in the registry?
The registry currently lists 1 device for Geyser S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geyser S.A.'s devices?
Among its 1 most recently registered device, Geyser S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Geyser S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Geyser S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geyser S.A. in the registry?
The most recently registered devices listed for Geyser S.A. include ENDOBOY.