Innolux Corporation
TaiwanFDA applicant, unverified
- Devices
- 1
What Innolux Corporation makes
Innolux Corporation manufactures the Innolux RIC, a reusable infusion catheter designed for intravenous administration of fluids and medications. This device is intended for use in clinical settings to facilitate reliable and secure vascular access during medical procedures.
The Innolux RIC falls under FDA Class II regulation and has been authorised through the 510(k) clearance process. The company is based in the United States, and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Innolux Ric Ref K162344
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innolux Corporation have in the registry?
The registry currently lists 1 device for Innolux Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innolux Corporation's devices?
Among its 1 most recently registered device, Innolux Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Innolux Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Innolux Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innolux Corporation in the registry?
The most recently registered devices listed for Innolux Corporation include INNOLUX RIC.