Mecon Labs
Country not established
- Devices
- 2
What Mecon Labs makes
Mecon Labs manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the MECON X and MECON I models, designed for pain management and muscle stimulation.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mecon X (Ten) Ref K843484
Regimes: 510(k) Registry: 510(k)Mecon I Ref K823788
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mecon Labs have in the registry?
The registry currently lists 2 devices for Mecon Labs. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mecon Labs's devices?
Among its 2 most recently registered devices, Mecon Labs has devices listed in FDA 510(k) (2 devices).
What risk classes do Mecon Labs's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mecon Labs's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mecon Labs in the registry?
The most recently registered devices listed for Mecon Labs include MECON X (TEN) and MECON I.