Lantor Group
United KingdomFDA applicant, unverified
- Devices
- 1
What Lantor Group makes
The company produces the Lantor Cube Sterilizer Test Pack, a device designed for validating and testing the performance of autoclave sterilizers in healthcare and laboratory settings.
This product is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lantor Cube Sterilizer Test Pack Ref K882756
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lantor Group have in the registry?
The registry currently lists 1 device for Lantor Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lantor Group's devices?
Among its 1 most recently registered device, Lantor Group has devices listed in FDA 510(k) (1 device).
What risk classes do Lantor Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lantor Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lantor Group in the registry?
The most recently registered devices listed for Lantor Group include LANTOR CUBE STERILIZER TEST PACK.