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Dr. Renú SpectraLift Advanced

The only device in this set that publishes a per-mode irradiance range, names the instrument used and puts a document behind it. Two caveats sit alongside that: the clearance is held by the OEM and covers wrinkle reduction only, and in the EU the device is explicitly not CE-marked as a medical device.

Dr. RenúUpdated 2026-09-18Measurement queued
Measurement status

This device has not been measured yet. Nothing on this page is presented as a measurement, and no irradiance figure here has been verified by us.

Specification

Origin

The Dr. Renú SpectraLift Advanced is manufactured in China. The FDA-registered manufacturing establishment for this device platform is located in Shenzhen, Guangdong, China. Source: FDA Establishment Registration & Device Listing database.

What the regulatory status actually means

Dr. Renú SpectraLift Advanced holds an FDA 510(k) clearance. Clearance means the manufacturer showed the device is substantially equivalent to one already on the market. It is not FDA approval, and it is not evidence that the device works for any particular person.

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