Fluoptics
Country not established
Part of Fluoptics SAS
Fluoptics is a medical device manufacturer, with 18 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 18
Registry facts
- Registries
- FDA GUDID 16
- FDA 510(k) 2
- Device classes
- FDA Class II 14
- FDA Class I 4
- Sites and related companies
- Identifiers
- DUNS 260631677
Catalogue
Search and filter all 18 devicesCompany details
- DUNS number
- 260631677
Frequently asked questions
How many devices does FLUOPTICS have in the registry?
The registry currently lists 18 devices for FLUOPTICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list FLUOPTICS's devices?
Among its 18 most recently registered devices, FLUOPTICS has devices listed in FDA 510(k) (2 devices) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do FLUOPTICS's devices fall under?
Among its 18 most recently registered devices, the classes recorded for FLUOPTICS's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from FLUOPTICS in the registry?
The most recently registered devices listed for FLUOPTICS include PHOTONVUE PVUEC0A2 V1.0, FLUOCASE 800 FC800-CL v1.9, FLUOBEAM SYSTEM STORED INTO FLUOBOX FX-CL v1.1 and FLUOBEAM 800 FB800-CL v1.8.