Cordis Corp., A Johnson & Johnson Co.
United StatesFDA applicant, unverified
- Devices
- 11
What Cordis Corp., A Johnson & Johnson Co. makes
Cordis Corp. manufactures vascular interventional devices, including re-entry catheters like the OUTBACK LTD for treating chronic total occlusions, emboli capture guidewires such as the ANGIOGUARD XP and RX for preventing stroke during procedures, and retrievable inferior vena cava filters like the OPTEASE. The portfolio also includes guiding catheters, such as the ADROIT and MICRO GUIDE CATHETER ELITE, designed for precise delivery of therapeutic agents or devices in coronary and peripheral vascular interventions.
The company’s devices are classified under FDA Class II and are authorised via the 510(k) pathway. Products are listed with the U.S. Food and Drug Administration under this regulatory framework. The manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Cordis Corp., A Johnson & Johnson Co. have in the registry?
The registry currently lists 11 devices for Cordis Corp., A Johnson & Johnson Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cordis Corp., A Johnson & Johnson Co.'s devices?
Among its 11 most recently registered devices, Cordis Corp., A Johnson & Johnson Co. has devices listed in FDA 510(k) (11 devices).
What risk classes do Cordis Corp., A Johnson & Johnson Co.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Cordis Corp., A Johnson & Johnson Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cordis Corp., A Johnson & Johnson Co. in the registry?
The most recently registered devices listed for Cordis Corp., A Johnson & Johnson Co. include OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120, OUTBACK Elite Re-Entry Catheter, CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE and OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER.