Kimed Industries, Inc.
Country not established
- Devices
- 1
What Kimed Industries, Inc. makes
Kimed Industries, Inc. manufactures the AGAR 8000 TENS, a transcutaneous electrical nerve stimulation (TENS) device designed for pain management applications.
The AGAR 8000 TENS is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Agar 8000 Tens Ref K832851
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kimed Industries, Inc. have in the registry?
The registry currently lists 1 device for Kimed Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kimed Industries, Inc.'s devices?
Among its 1 most recently registered device, Kimed Industries, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kimed Industries, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kimed Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kimed Industries, Inc. in the registry?
The most recently registered devices listed for Kimed Industries, Inc. include AGAR 8000 TENS.