Ari
Country not established
- Devices
- 1
What Ari makes
Ari manufactures the ARI Cold Spray, a device designed for rapid cooling and pain relief in acute medical settings, typically applied to injuries or post-procedural sites.
The ARI Cold Spray is classified as a Class II (U) device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ari Cold Spray Ref K033720
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ari have in the registry?
The registry currently lists 1 device for Ari. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ari's devices?
Among its 1 most recently registered device, Ari has devices listed in FDA 510(k) (1 device).
What are the newest devices from Ari in the registry?
The most recently registered devices listed for Ari include ARI COLD SPRAY.