Microstim, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Microstim, Inc. makes
Microstim, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the MICROSTIM 100 Model 2C and the MICROSTIM 100I, designed for pain management through low-voltage electrical stimulation.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Microstim 100 Model 2C Ref K910580
Regimes: 510(k) Registry: 510(k)Microstim 100I Tens Device Ref K010295
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microstim, Inc. have in the registry?
The registry currently lists 2 devices for Microstim, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microstim, Inc.'s devices?
Among its 2 most recently registered devices, Microstim, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Microstim, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Microstim, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microstim, Inc. in the registry?
The most recently registered devices listed for Microstim, Inc. include MICROSTIM 100 MODEL 2C and MICROSTIM 100I TENS DEVICE.