Jomed AG
Country not established
- Devices
- 9
What Jomed AG makes
Jomed AG manufactures peripheral angioplasty catheters, including the FOX PTA Catheter in sizes 3.0 to 8.0 x 40 mm, and modifications thereof. The company also produces the JOSTENT SELFX stent, available in multiple model variants for vascular applications.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Jomed AG operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Smartwire/Smartmap Pressure System Ref K021219
Regimes: 510(k) Registry: 510(k)In-Vision Imaging System Ref K031148
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Modification To Fox Pta Catheter Ref K020854
Regimes: 510(k) Registry: 510(k)Trak Back Ii Ref K003938
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jomed AG have in the registry?
The registry currently lists 9 devices for Jomed AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jomed AG's devices?
Among its 9 most recently registered devices, Jomed AG has devices listed in FDA 510(k) (9 devices).
What risk classes do Jomed AG's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Jomed AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jomed AG in the registry?
The most recently registered devices listed for Jomed AG include JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000, AG141002, AG141010, AG14M060 & AG14M050, SMARTWIRE/SMARTMAP PRESSURE SYSTEM, IN-VISION IMAGING SYSTEM and FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, A14007, A14008.