Glottal Ent., Inc.
United Statesfrom the FDA registration address FDA FEI 1319182
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Electroglottograph Ref K901609
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1319182
- Address
- 1201 E. FAYETTE ST., SYRACUSE, NY, 13210
Frequently asked questions
How many devices does Glottal Ent., Inc. have in the registry?
The registry currently lists 1 device for Glottal Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glottal Ent., Inc.'s devices?
Among its 1 most recently registered device, Glottal Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Glottal Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Glottal Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glottal Ent., Inc. in the registry?
The most recently registered devices listed for Glottal Ent., Inc. include ELECTROGLOTTOGRAPH.