Oms Medico, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Oms Medico, Inc. makes
Oms Medico, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including models such as the TX-2, NEU-PULS Model #295, UNI-PULS Model #292, GLOBALCARE, TX-3, TX-4 (SIGMA TENS), and 120Z. These devices are designed to deliver low-voltage electrical pulses for pain management and muscle stimulation.
The company’s TENS devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Tx-2(Tens) Ref K874333
Regimes: 510(k) Registry: 510(k)Neu-Puls(Tens) Model #295 Ref K870583
Regimes: 510(k) Registry: 510(k)Uni-Puls(Tens) Model #292 Ref K865063
Regimes: 510(k) Registry: 510(k)Globalcare(Tens) Ref K873420
Regimes: 510(k) Registry: 510(k)Tx-3(Tens) Ref K871699
Regimes: 510(k) Registry: 510(k)Tx-4(Tens) (Sigma Tens) Ref K874550
Regimes: 510(k) Registry: 510(k)120Z(Tens) Ref K873484
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oms Medico, Inc. have in the registry?
The registry currently lists 7 devices for Oms Medico, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oms Medico, Inc.'s devices?
Among its 7 most recently registered devices, Oms Medico, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Oms Medico, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Oms Medico, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oms Medico, Inc. in the registry?
The most recently registered devices listed for Oms Medico, Inc. include TX-2(TENS), NEU-PULS(TENS) MODEL #295, UNI-PULS(TENS) MODEL #292 and GLOBALCARE(TENS).