Nunc, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Nunc, Inc. makes
Nunc, Inc. manufactures single-use containers designed for cell culture applications, including tissue culture flasks, tubes, and dishes. These products are intended for use in laboratory settings to grow and maintain cells for research and bioprocessing purposes.
The company’s portfolio is classified under FDA’s Class I regulatory category, with devices listed via the 510(k) pathway. These products are intended for use in the United States, where they are subject to FDA oversight.
Catalogue
Tissue Culture Flasks Ref K873890
Regimes: 510(k) Registry: 510(k)Tissue Culture Tubes Ref K873889
Regimes: 510(k) Registry: 510(k)Tissue Culture Dishes Ref K873891
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nunc, Inc. have in the registry?
The registry currently lists 3 devices for Nunc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nunc, Inc.'s devices?
Among its 3 most recently registered devices, Nunc, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Nunc, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Nunc, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nunc, Inc. in the registry?
The most recently registered devices listed for Nunc, Inc. include TISSUE CULTURE FLASKS, TISSUE CULTURE TUBES and TISSUE CULTURE DISHES.