Jazz Imaging, LLC
Also registered as Jazz Imaging, Jazz Imaging, LLC Dba Jazz Imaging
United StatesFDA applicant, unverified FDA FEI 3013503781
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
JAZZ Solo sensor Ref K213637
Regimes: 510(k) Registry: 510(k)Jazz Classic Ref K241495
Regimes: 510(k) Registry: 510(k)JAZZ SOLO Sensor Ref K163224
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3013503781
- DUNS number
- 079381473
- Address
- 1710 Zanker Rd, San Jose, CA, 95112
- [email protected]
- Phone
- 567-234-5299
Frequently asked questions
How many devices does Jazz Imaging, LLC have in the registry?
The registry currently lists 4 devices for Jazz Imaging, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jazz Imaging, LLC's devices?
Among its 4 most recently registered devices, Jazz Imaging, LLC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Jazz Imaging, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Jazz Imaging, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jazz Imaging, LLC in the registry?
The most recently registered devices listed for Jazz Imaging, LLC include Solo 10-001, JAZZ Solo sensor and Jazz Classic.