Cathera, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 107
What Cathera, Inc. makes
Cathera, Inc. manufactures a range of catheter devices, including the Phenom 17, Phenom 21, Phenom 27, and Phenom Plus catheters, designed for medical procedures requiring precise vascular access or intervention.
These devices are classified under Class II by regulatory authorities and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 107 devicesShowing 1-50 of 107
Company details
- DUNS number
- 080116681
- [email protected]
- Phone
- +1-949-837-3700
Frequently asked questions
How many devices does CATHERA, INC. have in the registry?
The registry currently lists 107 devices for CATHERA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CATHERA, INC.'s devices?
Among its 50 most recently registered devices, CATHERA, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do CATHERA, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for CATHERA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CATHERA, INC. in the registry?
The most recently registered devices listed for CATHERA, INC. include Phenom™ Catheter FG11150-1015-2RV01, Phenom™ Catheter FG19120-0630-1SV02, Phenom™ Catheter FG11170-0615-2RV02 and Phenom™ Catheter FG19105-0630-1SV02.