Zbeats, Inc.
United StatesFDA 510(k) applicant, unverified FDA FEI 3031570367
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
ZBPro Diagnostic (Version 2.0) Ref K261580
510(k) 510(k)ZBPro Diagnostic Ref K243252
510(k) 510(k)
Company details
- FDA FEI number
- 3031570367
- Address
- 1500 Stony Brook Rd, Stony Brook, NY, 11794
Frequently asked questions
How many devices does Zbeats, Inc. have in the registry?
The registry currently lists 2 devices for Zbeats, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zbeats, Inc.'s devices?
Among its 2 most recently registered devices, Zbeats, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Zbeats, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Zbeats, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zbeats, Inc. in the registry?
The most recently registered devices listed for Zbeats, Inc. include ZBPro Diagnostic (Version 2.0) and ZBPro Diagnostic.