Fiab SpA
ItalyFDA 510(k) applicant, unverified FDA FEI 3003072803
- Devices
- 57
- Registrations
- FDA
- FDA recalls
- 0
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 devicesFiab SpA, Models F7244, F7233, F7234, F7277 Ref K100333
CE MDR 510(k) 510(k)- CE MDR 510(k) 510(k)
- 510(k) 510(k)
- CE MDR 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
Showing 51-57 of 57
Company details
- FDA FEI number
- 3003072803
- DUNS number
- 439770017
- Address
- Via Costoli, 4, Vicchio Firenze
- [email protected]
- Phone
- +39 0558497943