Curomatic, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Curomatic, Inc. makes
Curomatic, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the TENS-O-TEST, designed for pain management applications. These devices deliver low-voltage electrical currents to the skin to alleviate discomfort in targeted areas.
The company’s portfolio is regulated under Class II medical devices in the United States, with devices authorised through the FDA’s 510(k) clearance process. The manufacturer operates from the US.
Catalogue
Tens-O-Test Ref K791637
510(k) 510(k)Tens-O-Test Ref K781321
510(k) 510(k)
Frequently asked questions
How many devices does Curomatic, Inc. have in the registry?
The registry currently lists 2 devices for Curomatic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curomatic, Inc.'s devices?
Among its 2 most recently registered devices, Curomatic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Curomatic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Curomatic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curomatic, Inc. in the registry?
The most recently registered devices listed for Curomatic, Inc. include TENS-O-TEST.