Blaine Labs, Inc.
United Statesfrom the FDA registration address FDA FEI 3001744192
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Blaine Scarcare Patch Ref K001608
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001744192
- Address
- 11037 LOCKPORT PLACE, SANTA FE SPRINGS, CA, 90670
Frequently asked questions
How many devices does Blaine Labs, Inc. have in the registry?
The registry currently lists 1 device for Blaine Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blaine Labs, Inc.'s devices?
Among its 1 most recently registered device, Blaine Labs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Blaine Labs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Blaine Labs, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Blaine Labs, Inc. in the registry?
The most recently registered devices listed for Blaine Labs, Inc. include BLAINE SCARCARE PATCH.