Inpeco S.p.A.
ItalyFDA applicant, unverified FDA FEI 3005509212
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Inpeco S.p.A. makes
Inpeco S.P.A. manufactures laboratory automation systems, including the FLEXLAB 3.6 and the ACCELERATOR A3600.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Flexlab 3.6, Accelerator A3600 Ref K121012
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005509212
- Address
- Via Givoletto 15, Val della Torre Torino
Frequently asked questions
How many devices does Inpeco S.P.A. have in the registry?
The registry currently lists 1 device for Inpeco S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inpeco S.P.A.'s devices?
Among its 1 most recently registered device, Inpeco S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Inpeco S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Inpeco S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inpeco S.P.A. in the registry?
The most recently registered devices listed for Inpeco S.P.A. include FLEXLAB 3.6, ACCELERATOR A3600.