Hinlab SAS
Also registered as Hinlab, Inc.
United Statesfrom the FDA registration address FDA FEI 3044675072
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pediarity™ Ref K231531
Regimes: 510(k) Registry: 510(k)Hinscope Ref K241397
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3044675072
- Address
- 412 Canary Ct, Lewes, DE, 19958
Frequently asked questions
How many devices does Hinlab Sas have in the registry?
The registry currently lists 2 devices for Hinlab Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hinlab Sas's devices?
Among its 2 most recently registered devices, Hinlab Sas has devices listed in FDA 510(k) (2 devices).
What risk classes do Hinlab Sas's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hinlab Sas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hinlab Sas in the registry?
The most recently registered devices listed for Hinlab Sas include Pediarity™ and Hinscope.