Rouge Ent., Inc.
Country not established
- Devices
- 1
What Rouge Ent., Inc. makes
Rouge Ent., Inc. manufactures patient examination gloves made of latex.
The company's products are Class I devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves (Latex) Ref K892273
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rouge Ent., Inc. have in the registry?
The registry currently lists 1 device for Rouge Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rouge Ent., Inc.'s devices?
Among its 1 most recently registered device, Rouge Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rouge Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rouge Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rouge Ent., Inc. in the registry?
The most recently registered devices listed for Rouge Ent., Inc. include PATIENT EXAMINATION GLOVES (LATEX).