Koalaty Products, Inc.
Country not established
- Devices
- 3
What Koalaty Products, Inc. makes
Koalaty Products, Inc. makes transcutaneous electrical nerve stimulation (TENS) devices and electrical muscle stimulation (EMS) devices, including models such as the TENS Stimulator 2800 and 3000, TENS 7000, EMS 7500, Twin Stim, EMS 5.0, and EMS 5.1.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Tens Stimulator, Models 2800 And 3000 Ref K102014
Regimes: 510(k) Registry: 510(k)Models Tens 7000, Ems 7500 And Twin Stim Ref K080661
Regimes: 510(k) Registry: 510(k)Models Ems 5.0, Ems 5.1 Ref K072795
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Koalaty Products, Inc. have in the registry?
The registry currently lists 3 devices for Koalaty Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koalaty Products, Inc.'s devices?
Among its 3 most recently registered devices, Koalaty Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Koalaty Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Koalaty Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Koalaty Products, Inc. in the registry?
The most recently registered devices listed for Koalaty Products, Inc. include TENS STIMULATOR, MODELS 2800 AND 3000, MODELS TENS 7000, EMS 7500 AND TWIN STIM and MODELS EMS 5.0, EMS 5.1.