Geno Laboratories
Country not established
- Devices
- 1
What Geno Laboratories makes
Geno Laboratories manufactures ultrasound coupling gel, a medium applied between ultrasound transducers and skin to enhance imaging clarity and reduce friction during scans.
The company’s ultrasound coupling gel is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The product is registered in the United States.
Catalogue
Ultrasound Coupling Gel Ref K904418
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geno Laboratories have in the registry?
The registry currently lists 1 device for Geno Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geno Laboratories's devices?
Among its 1 most recently registered device, Geno Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Geno Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Geno Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geno Laboratories in the registry?
The most recently registered devices listed for Geno Laboratories include ULTRASOUND COUPLING GEL.