Eele Laboratories, LLC
Country not established
- Devices
- 1
What Eele Laboratories, LLC makes
Eele Laboratories, LLC manufactures the PLASMACURE BXE, a device designed for plasma treatment applications in medical or laboratory settings, likely used for sterilization or surface modification processes.
The PLASMACURE BXE is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Plasmacure Bxe Ref K033795
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eele Laboratories, LLC have in the registry?
The registry currently lists 1 device for Eele Laboratories, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eele Laboratories, LLC's devices?
Among its 1 most recently registered device, Eele Laboratories, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Eele Laboratories, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eele Laboratories, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eele Laboratories, LLC in the registry?
The most recently registered devices listed for Eele Laboratories, LLC include PLASMACURE BXE.