Luminoah
United Statesfrom the FDA registration address FDA FEI 3046434077
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Luminoah makes
Luminoah manufactures the FLOW™ Enteral Nutrition System, a device designed for administering enteral nutrition to patients requiring tube feeding support.
The FLOW™ Enteral Nutrition System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Luminoah FLOW™ Enteral Nutrition System Ref K253558
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046434077
- Address
- 1 Morton Dr Ste 100, Charlottesville, VA, 22903
Frequently asked questions
How many devices does Luminoah have in the registry?
The registry currently lists 1 device for Luminoah. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luminoah's devices?
Among its 1 most recently registered device, Luminoah has devices listed in FDA 510(k) (1 device).
What risk classes do Luminoah's devices fall under?
Among its 1 most recently registered device, the classes recorded for Luminoah's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luminoah in the registry?
The most recently registered devices listed for Luminoah include Luminoah FLOW™ Enteral Nutrition System.