Rogo Ent.
Country not established
- Devices
- 1
What Rogo Ent. makes
Rogo Ent. manufactures the STERI-TRACT, a medical device designed for sterilization and tract cleaning in specific surgical or procedural applications.
The STERI-TRACT is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Steri-Tract Ref K811863
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rogo Ent. have in the registry?
The registry currently lists 1 device for Rogo Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rogo Ent.'s devices?
Among its 1 most recently registered device, Rogo Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Rogo Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rogo Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rogo Ent. in the registry?
The most recently registered devices listed for Rogo Ent. include STERI-TRACT.