Earflo, Inc.
United Statesfrom the FDA registration address FDA FEI 3043739646
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Earflo (EF001) Ref K252751
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043739646
- DUNS number
- 138345369
- Address
- 203 Lothrop St, Pittsburgh, PA, 15213
- [email protected]
- Phone
- 8054527453
Frequently asked questions
How many devices does Earflo, Inc. have in the registry?
The registry currently lists 2 devices for Earflo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Earflo, Inc.'s devices?
Among its 2 most recently registered devices, Earflo, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from Earflo, Inc. in the registry?
The most recently registered devices listed for Earflo, Inc. include Earflo EF001 and Earflo (EF001).