M&S Technologies
United States US-MF-000048924 Last updated 23 Oct 2026
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- Devices
- 2
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
M&S Technologies Clinical Trial Suite® Ref CTS-1500-HR
Related companies
Authorised representatives
What M&S Technologies makes
M&S Technologies produces the Smart System® Virtual Reality Headset System and the Clinical Trial Suite®, both of which are Class I medical devices.
The company is based in the US and its devices are listed in the EUDAMED registry.
Frequently asked questions
What medical devices does M&S Technologies produce?
M&S Technologies produces the Smart System® Virtual Reality Headset System and the Clinical Trial Suite®, both of which are Class I medical devices designed for specific clinical applications.
Where is M&S Technologies based?
M&S Technologies is based in the United States, with its operations and manufacturing facilities located within the country.
Which regulatory registries list M&S Technologies' devices?
M&S Technologies' devices are listed in the EUDAMED registry, which is the European database for medical devices, though they may also be listed in other regional registries depending on market authorization.
How are M&S Technologies' devices classified?
M&S Technologies' devices, including the Smart System® Virtual Reality Headset System and Clinical Trial Suite®, are classified as Class I medical devices, which are the lowest risk category in regulatory classifications.
Information
- Country
- United States
- Address
- 5715, W Howard St, Niles, United States
- Website
- mstech-eyes.com/
- [email protected]
- Phone
- +17749871008; ext=3008
- PRRC contact
- David Hufnagle
- EUDAMED SRN
- US-MF-000048924
- FDA FEI number
- 1000431353