Ichor
Country not established
- Devices
- 2
What Ichor makes
Ichor manufactures embolectomy systems designed for the removal of blood clots within blood vessels, including the ICHOR 14F and ICHOR 7F (ICH-7F) models. These devices are intended for use in interventional cardiology and vascular procedures to restore blood flow in cases of acute occlusion.
The company’s embolectomy systems fall under FDA Class II regulatory classification and are listed via the 510(k) pathway. These devices are authorised for commercial distribution in the United States, where Ichor is based.
Catalogue
ICHOR 14F Embolectomy System Ref K230743
Regimes: 510(k) Registry: 510(k)ICHOR 7F Embolectomy System (ICH-7F) Ref K233917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ichor have in the registry?
The registry currently lists 2 devices for Ichor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ichor's devices?
Among its 2 most recently registered devices, Ichor has devices listed in FDA 510(k) (2 devices).
What risk classes do Ichor's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ichor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ichor in the registry?
The most recently registered devices listed for Ichor include ICHOR 14F Embolectomy System and ICHOR 7F Embolectomy System (ICH-7F).