Certificates
Certified for professional use.
What each mark on a Visbody device means, in plain words.
- FDA registered (2026)
FDA registered
Listed for M50 · M60 · T55
Shenzhen Visbody is registered as a device establishment with the US Food and Drug Administration, registration number 3025421686, and lists the Visbody-M50, Visbody-M60 and Visbody-T55 as devices. This is an establishment registration and device listing. It is not an FDA approval or clearance of the device.
CE-EMC
Listed for M50 · M60 · T55
The device meets European rules on electromagnetic compatibility: it should not disturb other equipment and should keep working normally near it.
CE-LVD
Listed for M50 · M60 · T55
The device meets the European Low Voltage Directive, the safety rules for electrical equipment that runs on mains power.
FCC
Listed for M50 · M60 · T55
The device meets the limits set by the US Federal Communications Commission for radio-frequency emissions. On the T55 this includes Part 15B, declared through an SDoC (supplier's declaration of conformity).
RoHS
Listed for M60 · T55
The device follows the Restriction of Hazardous Substances rules, which limit certain substances in electrical equipment. On the T55 this covers the mirror and the turntable.
EN
Listed for T55
European Norms (EN) are harmonised European standards. They describe how equipment should be built and tested.
The CE and FCC Part 15B verifications cover the Visbody M50 and M60. RoHS for the M50 is available on request, because the RoHS certificate on file covers the M60. Certificates can change, so ask 4Select for the current details of the model you are considering.
Reports are for reference, not a medical diagnosis.
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