G-Flex Europe Sprl
BelgiumFDA 510(k) applicant, unverified
- Devices
- 1
What G-Flex Europe Sprl makes
G-Flex Europe Sprl manufactures Cysto-Gastro-Sets, which are reusable surgical instrument sets designed for cystoscopic and gastroscopic procedures. These sets include instruments and accessories used in urological and gastrointestinal examinations, such as biopsy forceps, graspers, and irrigation tools.
The company’s products fall under FDA Class II devices and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Cysto-Gastro-Sets Ref K211909
510(k) 510(k)
Frequently asked questions
How many devices does G-Flex Europe Sprl have in the registry?
The registry currently lists 1 device for G-Flex Europe Sprl. Devices recorded under merged duplicate company entries are counted once.
Which registries list G-Flex Europe Sprl's devices?
Among its 1 most recently registered device, G-Flex Europe Sprl has devices listed in FDA 510(k) (1 device).
What risk classes do G-Flex Europe Sprl's devices fall under?
Among its 1 most recently registered device, the classes recorded for G-Flex Europe Sprl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from G-Flex Europe Sprl in the registry?
The most recently registered devices listed for G-Flex Europe Sprl include Cysto-Gastro-Sets.