Soprane S.A.
Country not established
- Devices
- 1
What Soprane S.A. makes
Soprane S.A. manufactures Fertiloscopy kits, including models FH 1.29 and FTO 1.40, designed for diagnostic and therapeutic procedures in reproductive medicine.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Fertiloscopy Kit Fh 1.29/Fto 1.40 Ref K992655
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Soprane S.A. have in the registry?
The registry currently lists 1 device for Soprane S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Soprane S.A.'s devices?
Among its 1 most recently registered device, Soprane S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Soprane S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Soprane S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Soprane S.A. in the registry?
The most recently registered devices listed for Soprane S.A. include FERTILOSCOPY KIT FH 1.29/FTO 1.40.