Vetex Medical, Ltd.
IrelandFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Vetex Medical, Ltd. makes
Vetex Medical, Ltd. manufactures the ReVene Thrombectomy Catheter, a medical device used for thrombectomy procedures.
The ReVene Thrombectomy Catheter is classified as a Class II device and is listed in the FDA 510(k) registry. Vetex Medical, Ltd. is based in the US.
Catalogue
ReVene Thrombectomy Catheter Ref K201705
510(k) 510(k)
FDA establishments
- Vetex Medical Limited Ballinasloe Galway(County) · IE FEI 3014787927
Frequently asked questions
How many devices does Vetex Medical, Ltd. have in the registry?
The registry currently lists 1 device for Vetex Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vetex Medical, Ltd.'s devices?
Among its 1 most recently registered device, Vetex Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Vetex Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vetex Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vetex Medical, Ltd. in the registry?
The most recently registered devices listed for Vetex Medical, Ltd. include ReVene Thrombectomy Catheter.
Which FDA establishments are linked to Vetex Medical, Ltd.?
1 FDA establishment is linked to Vetex Medical, Ltd. in the registry; they are listed on the company page.