Meridia 12 Corp.
Country not established
- Devices
- 1
What Meridia 12 Corp. makes
Meridia 12 Corp. manufactures electroneural stimulators, including the ELECTRONEURAL STIMULATOR 12, designed for targeted nerve stimulation applications.
The company’s portfolio is regulated under Class II devices in the US and listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Electroneural Stimulator 12 Ref K831487
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meridia 12 Corp. have in the registry?
The registry currently lists 1 device for Meridia 12 Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meridia 12 Corp.'s devices?
Among its 1 most recently registered device, Meridia 12 Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Meridia 12 Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Meridia 12 Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meridia 12 Corp. in the registry?
The most recently registered devices listed for Meridia 12 Corp. include ELECTRONEURAL STIMULATOR 12.