ONDA PRO clinical images
What these images are
These are photographs supplied by the manufacturer of ONDA PRO, taken by clinicians in their own practices. Each one is credited to the person who supplied it. They document the use the clearance describes — the appearance of cellulite across the thighs and buttocks — and nothing beyond it.
What they are not
They are not Minori patients, and we will not present them as if they were. Our own before-and-after photographs live on the results page and are marked as ours. We also hold a further nineteen images from the same library that we have chosen not to publish, because what they show would suggest claims this clearance does not support.
Every image below was supplied by Cartessa Aesthetics, the distributor of ONDA PRO, and each carries the treating clinician's name printed on the image itself. They show patients treated at other clinics, not at Minori. Individual results vary.
Thighs and buttocks
The area the clearance speaks to: a temporary reduction in the appearance of cellulite.




Abdomen and waist
Supplied by the manufacturer for this area. ONDA PRO's FDA clearance (K260647) covers tissue heating and the appearance of cellulite; it does not list this area. Individual results may vary.




Face, jawline and neck
Supplied by the manufacturer for this area. ONDA PRO's FDA clearance (K260647) covers tissue heating and the appearance of cellulite; it does not list this area. Individual results may vary.












Upper arms
Supplied by the manufacturer for this area. ONDA PRO's FDA clearance (K260647) covers tissue heating and the appearance of cellulite; it does not list this area. Individual results may vary.

ONDA PRO, cleared as SPECCHIO, is FDA cleared for heating for the purpose of elevating tissue temperature for selected medical conditions such as temporary relief of pain, muscle spasms, and increase in local circulation — and, via the massage device, a temporary reduction in the appearance of cellulite. 510(k) K260647
Aesthetic devices are cleared under FDA 510(k), which is not the same as approved. We cite the clearance so you can read the indication yourself. It describes the device, not any individual result — outcomes vary, and a consultation is what determines whether a treatment suits you.
