Fiab SpA
ItalyFDA 510(k) applicant, unverified FDA FEI 3003072803
- Devices
- 57
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Fiab SpA makes
The company manufactures oesophageal temperature monitoring devices, including reusable and single-use probes, as well as dedicated monitors for clinical use. It also produces reusable electrical connection cables for medical devices and single-use electrocardiographic electrodes. Battery-powered cautery devices are part of its portfolio, designed for surgical procedures.
These products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and UDI databases. The company operates from the United States, adhering to applicable regulatory standards for electrical, reusable, and single-use medical devices.
Catalogue
Search and filter all 57 devicesShowing 1-50 of 57
Company details
- FDA FEI number
- 3003072803
- DUNS number
- 439770017
- Address
- Via Costoli, 4, Vicchio Firenze
- [email protected]
- Phone
- +39 0558497943
Frequently asked questions
How many devices does FIAB SPA have in the registry?
The registry currently lists 57 devices for FIAB SPA. Devices recorded under merged duplicate company entries are counted once.
Which registries list FIAB SPA's devices?
Among its 50 most recently registered devices, FIAB SPA has devices listed in EUDAMED (1 device) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do FIAB SPA's devices fall under?
Among its 50 most recently registered devices, the classes recorded for FIAB SPA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from FIAB SPA in the registry?
The most recently registered devices listed for FIAB SPA include NA F9053/41, NA F9024ONI, NA A113 and NA F9015SSC/RU.