Applied Fiberoptics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Applied Fiberoptics, Inc. makes
Applied Fiberoptics, Inc. manufactures flexible cystoscopes, flexible ureteroscopes, and nasal instruments for medical use.
The company's devices are regulated as Class I and Class II and are listed in the FDA 510(k) registry. Applied Fiberoptics, Inc. is based in the US.
Catalogue
Flexible Cystoscope Ref K964037
Regimes: 510(k) Registry: 510(k)Flexible Ureteroscope Ref K964482
Regimes: 510(k) Registry: 510(k)Nasal Instruments Ref K820621
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Fiberoptics, Inc. have in the registry?
The registry currently lists 3 devices for Applied Fiberoptics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Fiberoptics, Inc.'s devices?
Among its 3 most recently registered devices, Applied Fiberoptics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Applied Fiberoptics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Applied Fiberoptics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Fiberoptics, Inc. in the registry?
The most recently registered devices listed for Applied Fiberoptics, Inc. include FLEXIBLE CYSTOSCOPE, FLEXIBLE URETEROSCOPE and NASAL INSTRUMENTS.