Geno, LLC
Country not established
- Devices
- 1
What Geno, LLC makes
Geno, LLC manufactures the GENOSYL MV-1000, a medical device designed for molecular diagnostics, specifically targeting genetic analysis of microbial pathogens.
The GENOSYL MV-1000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Genosyl Mv-1000 Ref K120216
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geno, LLC have in the registry?
The registry currently lists 1 device for Geno, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geno, LLC's devices?
Among its 1 most recently registered device, Geno, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Geno, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Geno, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geno, LLC in the registry?
The most recently registered devices listed for Geno, LLC include GENOSYL MV-1000.