Nsk America Corp.
United StatesFDA applicant, unverified FDA FEI 1000139790
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Nsk America Corp. makes
NSK America Corp. manufactures dental spray devices, including the PANA SPRAY PLUS and PANA-SPRAY, designed for oral irrigation and rinsing applications in dental procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Pana Spray Plus Ref K131014
Regimes: 510(k) Registry: 510(k)Pana-Spray Ref K052700
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000139790
- Address
- 1800 Global Parkway, Hoffman Est, IL, 60192
Frequently asked questions
How many devices does Nsk America Corp. have in the registry?
The registry currently lists 2 devices for Nsk America Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nsk America Corp.'s devices?
Among its 2 most recently registered devices, Nsk America Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nsk America Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nsk America Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nsk America Corp. in the registry?
The most recently registered devices listed for Nsk America Corp. include PANA SPRAY PLUS and PANA-SPRAY.