Zenflow, Inc.
Country not established FDA FEI 3014211785
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
Zenflow Spring Scope Ref K251140
510(k) 510(k)Zenflow Spring® Implant and Delivery System Ref P250007
PMA PMA
Company details
- FDA FEI number
- 3014211785
- DUNS number
- 079412969
- Address
- 395 Oyster Point Blvd., South San Francisco, CA, 94080
- [email protected]
- Phone
- 650-419-7557
Frequently asked questions
How many devices does Zenflow, Inc. have in the registry?
The registry currently lists 8 devices for Zenflow, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zenflow, Inc.'s devices?
Among its 8 most recently registered devices, Zenflow, Inc. has devices listed in FDA 510(k) (1 device), FDA PMA (1 device) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Zenflow, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Zenflow, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Zenflow, Inc. in the registry?
The most recently registered devices listed for Zenflow, Inc. include Zenflow Spring® Implant and Delivery System ZFS-IMP-15-01, Zenflow Spring® Implant and Delivery System ZFS-IMP-18-01, Zenflow Spring® Implant and Delivery System ZFS-IMP-21-01 and Zenflow Spring® Implant Retrieval Device ZFS-IRD-01.