The Reflux Company
Country not established FDA establishment FEI 3039167637
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
Company details
- FDA FEI number
- 3039167637
- Address
- 7868 Silverton Ave Ste J, San Diego, CA, 92126
Frequently asked questions
How many devices does THE REFLUX COMPANY have in the registry?
The registry currently lists 4 devices for THE REFLUX COMPANY. Devices recorded under merged duplicate company entries are counted once.
Which registries list THE REFLUX COMPANY's devices?
Among its 4 most recently registered devices, THE REFLUX COMPANY has devices listed in FDA GUDID (4 devices).
What risk classes do THE REFLUX COMPANY's devices fall under?
Among its 4 most recently registered devices, the classes recorded for THE REFLUX COMPANY's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from THE REFLUX COMPANY in the registry?
The most recently registered devices listed for THE REFLUX COMPANY include Reflux Band 101-1170-00, Reflux Band Pressure Sensor 101-1290-00, Reflux Band Manometer 101-250-00 and Secca 8000.