Nidek Incorporated
Country not established FDA establishment FEI 2936921
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Nidek Multicolor Laser Photocoagulator Ref K110228
510(k) 510(k)
Company details
- FDA FEI number
- 2936921
- Address
- 6601 Cascades Court, The Colony, TX, 75056
Frequently asked questions
How many devices does NIDEK INCORPORATED have in the registry?
The registry currently lists 1 device for NIDEK INCORPORATED. Devices recorded under merged duplicate company entries are counted once.
Which registries list NIDEK INCORPORATED's devices?
Among its 1 most recently registered device, NIDEK INCORPORATED has devices listed in FDA 510(k) (1 device).
What risk classes do NIDEK INCORPORATED's devices fall under?
Among its 1 most recently registered device, the classes recorded for NIDEK INCORPORATED's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NIDEK INCORPORATED in the registry?
The most recently registered devices listed for NIDEK INCORPORATED include NIDEK MULTICOLOR LASER PHOTOCOAGULATOR.