Uni-Patch, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Uni-Patch, Inc. makes
Uni-Patch, Inc. manufactures transcutaneous electrical nerve stimulation (TENS), functional electrical stimulation (FES), neuromuscular electrical stimulation (NMES) electrodes, including reusable and single-use models, as well as repositionable prewired TENS electrodes. The company also produces conductive gels for electrode adhesion and performance, such as aloe-based conductive gel in various packaging sizes.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Tantone Multi-Day #633 Tens Electrode Ref K871222
Regimes: 510(k) Registry: 510(k)Tens/Fes/Nmes Electrodes Ref K983097
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Tens/Fes/Nmes Electrodes Ref K962332
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Uni-Patch, Inc. have in the registry?
The registry currently lists 6 devices for Uni-Patch, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uni-Patch, Inc.'s devices?
Among its 6 most recently registered devices, Uni-Patch, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Uni-Patch, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Uni-Patch, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uni-Patch, Inc. in the registry?
The most recently registered devices listed for Uni-Patch, Inc. include EASY FLEX TENS/FES/MNS ELECTRODES 2 ROUND MODEL 8200/2X2 MODEL 8220, TANTONE MULTI-DAY #633 TENS ELECTRODE, TENS/FES/NMES ELECTRODES and CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON.