Fibra Sonics, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ultrasonic Lithotriptor 300A Ref K842024
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Phaco Fragmentor Gt-1 Ref K834453
Regimes: 510(k) Registry: 510(k)Lewicky Anterior Chamber Mainten. Sys. Ref K802381
Regimes: 510(k) Registry: 510(k)Ultrasonic Fragmentor Ref K813389
Regimes: 510(k) Registry: 510(k)Hygientist; Cycloson I & Ii; Retrofit Ref K812909
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Exonix Ref K984199
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fibra Sonics, Inc. have in the registry?
The registry currently lists 10 devices for Fibra Sonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fibra Sonics, Inc.'s devices?
Among its 10 most recently registered devices, Fibra Sonics, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Fibra Sonics, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Fibra Sonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fibra Sonics, Inc. in the registry?
The most recently registered devices listed for Fibra Sonics, Inc. include FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA, ULTRASONIC LITHOTRIPTOR 300A, FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000 and FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM.