Endocross, Ltd.
Country not established
- Devices
- 3
What Endocross, Ltd. makes
Endocross, Ltd. manufactures vascular catheters and catheter systems designed for interventional procedures, including the ENABLER-P Catheter, ENABLER-P Support Catheter, and the ENABLER-P Catheter System (Model 3000). These devices are intended for use in guiding and supporting medical instruments within blood vessels during treatments such as angioplasty or stent placement.
The company’s products fall under FDA Class II devices and are recorded in the 510(k) clearance registry. Endocross, Ltd. is based in the United States.
Catalogue
Enabler-P Catheter, 1000 Part NUMBER:1160 Ref K083833
Regimes: 510(k) Registry: 510(k)Enabler-P Support Catheter Ref K082339
Regimes: 510(k) Registry: 510(k)Enabler-P Catheter System, Model 3000 Ref K092174
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endocross, Ltd. have in the registry?
The registry currently lists 3 devices for Endocross, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endocross, Ltd.'s devices?
Among its 3 most recently registered devices, Endocross, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Endocross, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Endocross, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endocross, Ltd. in the registry?
The most recently registered devices listed for Endocross, Ltd. include ENABLER-P CATHETER, 1000 PART NUMBER:1160, ENABLER-P SUPPORT CATHETER and ENABLER-P CATHETER SYSTEM, MODEL 3000.