Corning Incorporated
United Statesfrom the FDA registration address FDA FEI 3011777678
- Devices
- 681
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Corning Incorporated makes
Corning Incorporated makes blood/tissue storage/culture containers.
Its devices are listed in the FDA GUDID device identification database. The listed devices are recorded across Class I and Class II.
Catalogue
Search and filter all 681 devicesShowing 1-50 of 681
Company details
- FDA FEI number
- 3011777678
- Address
- 836 North St Bldg 300 Ste 3401, Tewksbury, MA, 01876
- Website
- www.corning.com
Frequently asked questions
How many devices does Corning Incorporated have in the registry?
The registry currently lists 681 devices for Corning Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corning Incorporated's devices?
Among its 50 most recently registered devices, Corning Incorporated has devices listed in FDA GUDID (50 devices).
What risk classes do Corning Incorporated's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Corning Incorporated's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Corning Incorporated in the registry?
The most recently registered devices listed for Corning Incorporated include Corning 11090, Corning 11096, Corning 11504 and Corning 11513.