Ivion Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Ivion Corp. makes
Ivion Corp. manufactures port access catheters for long-term venous or arterial catheterization, including the SURECATH PORT ACCESS CATHETER. The company also produces intravenous administration sets with integrated flow clips, such as the IVION ADMIN SETS W/FLOW CLIPS, and programmable infusion pumps like the TRILOGY INFUSION PUMP, designed for controlled fluid delivery.
The company’s devices are classified under FDA Class II and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) registry. Ivion Corp. is based in the United States.
Catalogue
Surecath Port Access Catheter Ref K920036
Regimes: 510(k) Registry: 510(k)Ivion Admin Sets W/Flow Clips Ref K925219
Regimes: 510(k) Registry: 510(k)Trilogy Infusion Pump Ref K925311
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ivion Corp. have in the registry?
The registry currently lists 3 devices for Ivion Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ivion Corp.'s devices?
Among its 3 most recently registered devices, Ivion Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ivion Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ivion Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ivion Corp. in the registry?
The most recently registered devices listed for Ivion Corp. include SURECATH PORT ACCESS CATHETER, IVION ADMIN SETS W/FLOW CLIPS and TRILOGY INFUSION PUMP.