Medstar, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medstar, Inc. makes
Medstar, Inc. manufactures electrotherapy devices, including the SAFE-STRIPS for transcutaneous electrical nerve stimulation (TENS) and the INTERTRON 4500, INTERTRON 5000, and MASTERSTIM I-2 for neuromuscular electrical stimulation (NMES). These products are designed for pain management and muscle stimulation therapies.
The company’s portfolio is regulated under Class II medical devices in the US, with devices authorised through the FDA’s 510(k) clearance process. Medstar, Inc. is based in the United States.
Catalogue
Safe-Strips Ref K880548
Regimes: 510(k) Registry: 510(k)Intertron 4500, Intertron 5000, Masterstim I-2 Ref K921612
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medstar, Inc. have in the registry?
The registry currently lists 2 devices for Medstar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medstar, Inc.'s devices?
Among its 2 most recently registered devices, Medstar, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medstar, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medstar, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medstar, Inc. in the registry?
The most recently registered devices listed for Medstar, Inc. include SAFE-STRIPS and INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2.