Retech
Country not established
- Devices
- 1
What Retech makes
Retech manufactures an endoscopic sclerotherapy balloon, designed for medical procedures to treat vascular conditions by delivering sclerosing agents within blood vessels.
The company’s endoscopic sclerotherapy balloon is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Endoscopic Sclerotherapy Balloon Ref K821999
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retech have in the registry?
The registry currently lists 1 device for Retech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retech's devices?
Among its 1 most recently registered device, Retech has devices listed in FDA 510(k) (1 device).
What risk classes do Retech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Retech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retech in the registry?
The most recently registered devices listed for Retech include ENDOSCOPIC SCLEROTHERAPY BALLOON.