Axora Medical, Inc.
Country not established FDA FEI 3043236281
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
- GUDID
- GUDID
HERizon RD5 Resecting Device (5FR1PK) Ref K260984
510(k) 510(k)Minerva Endometrial Ablation System Ref P140013
PMA PMAGenesys Hta System Ref P000040
PMA PMA
Company details
- FDA FEI number
- 3043236281
- DUNS number
- 144943476
- Address
- 1000 Hamlin Ct, Sunnyvale, CA, 94089
- [email protected]
- Phone
- 855-646-7874
Frequently asked questions
How many devices does Axora Medical, Inc. have in the registry?
The registry currently lists 6 devices for Axora Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Axora Medical, Inc.'s devices?
Among its 6 most recently registered devices, Axora Medical, Inc. has devices listed in FDA 510(k) (1 device), FDA PMA (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Axora Medical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Axora Medical, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Axora Medical, Inc. in the registry?
The most recently registered devices listed for Axora Medical, Inc. include Resectr Resection Device 5FR (1.65 mm) M0065907051, Resectr Resection Device 9FR (3.0 mm) M0065907041, HERizon RD5 Resecting Device 5FR1PK and HERizon RD5 Resecting Device (5FR1PK).