Inter Med Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Inter Med Industries, Inc. makes
Inter Med Industries, Inc. manufactures external neuromuscular and transcutaneous electrical nerve stimulation devices, including the NEUROGAR III-TRANSCUT, NEUROGAR IV, and NEUROGAR III. These products are designed for pain management and muscle stimulation through electrical stimulation.
The company’s portfolio consists of Class II devices, each authorised via the FDA’s 510(k) clearance process. These devices are listed under the US regulatory framework and are based in the United States.
Catalogue
Neurogar Iii-Transcut. Elec. Nerve Stim Ref K801576
Regimes: 510(k) Registry: 510(k)Neurogar Iv-External Neuro-Muscle Stim. Ref K801577
Regimes: 510(k) Registry: 510(k)Neurogar Iii Ref K812036
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inter Med Industries, Inc. have in the registry?
The registry currently lists 3 devices for Inter Med Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inter Med Industries, Inc.'s devices?
Among its 3 most recently registered devices, Inter Med Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Inter Med Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Inter Med Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inter Med Industries, Inc. in the registry?
The most recently registered devices listed for Inter Med Industries, Inc. include NEUROGAR III-TRANSCUT. ELEC. NERVE STIM, NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. and NEUROGAR III.