Country + exact model
Confirm the manufacturer, country, full model name and applicator or mode. Similar names can refer to different generations.

Imaging · Applicator · Area · Risk · Follow-up
The official instructions distinguish imaging from treatment delivery and list contraindications and adverse events. A device name alone cannot select settings or establish suitability.
The Ulthera System with PRIME model combines ultrasound imaging with delivery of focused ultrasound that creates discrete thermal coagulation points. Official indications and clearances are device-, country- and area-specific. The physician must confirm the exact model, applicator, planned area, anatomy, contraindications, settings context, expected trade-offs, aftercare and review point.
General information only. It is not a diagnosis or a treatment recommendation. Individual suitability and response vary.
Open visible sourceDevice Program comparison
Use the same checklist for energy-based Programs so country, model, treatment area, settings basis, sessions, safety and total quotation remain comparable.
Confirm the manufacturer country and exact device model during consultation.Confirm the manufacturer, country, full model name and applicator or mode. Similar names can refer to different generations.
Match the concern and area to the mechanism. Compare the stated shot, line, pulse, energy, time or area basis instead of a headline number alone.
Compare assessment, operator, comfort or cooling plan, expected recovery, review point, planned sessions, aftercare and the full itemised quotation.
Decision aid
Do not transfer claims, images or protocols from Ultraformer MPT Program or legacy Ulthera SPT Program.
Ask for the exact Ulthera System model and the applicator planned for each area.
Confirm modelSeparate skin laxity, tissue position, volume and texture before discussing an energy plan.
Map the areaDiscuss pain, redness, swelling, bruising and the less-common events in the official instructions, plus the escalation route.
Request the safety planWhat happens next
A clear process reduces uncertainty before, during and after a Program.
Choose price, suitability, recovery, booking or a low-context photo/sticker start.
Review anatomy, history, previous procedures, contraindications and realistic alternatives.
Record the exact Program, device or product, area, technique or settings context, quotation and consent.
Receive written aftercare, an escalation route and a defined follow-up point.
Safety before booking
Suitability depends on the person, the exact Program and the locally available device, product and technique.
Tell the physician about allergies, medicines and supplements, pregnancy or breastfeeding, active infection, implanted devices and previous procedure reactions.
Do not stop or change prescribed medicine for a cosmetic appointment unless the prescribing clinician tells you to. Bring relevant records when available.
Before leaving, know who to contact for severe, unusual or worsening symptoms and when urgent medical assessment is needed.
Patient review and before-and-after images
This review gallery documents individual patients with before-and-after images and does not predict another person's outcome.

The image identifies the Program, but does not by itself establish the exact product variant, amount, treatment area, technique or complete treatment plan.
Individual results vary. Capture timing, lighting, expression, camera distance and angle may differ as part of real-world clinical photography. A physician consultation is required before treatment.

Questions from chat
The Ulthera System with PRIME model combines ultrasound imaging with delivery of focused ultrasound that creates discrete thermal coagulation points. Official indications and clearances are device-, country- and area-specific. The physician must confirm the exact model, applicator, planned area, anatomy, contraindications, settings context, expected trade-offs, aftercare and review point.
No. They are different device systems. Confirm the exact model, transducer or applicator, locally applicable use, settings context and evidence separately.
No. The official instructions list post-treatment effects and post-market adverse events, including edema, erythema, bruising, pain or burning and less-common complications. Individual risk requires assessment.
There is no universal count. The exact device, area, anatomy, goal, response and review determine whether another treatment is considered.
Citation continuity
Patient-visible copy and source links are the same for people and crawlers.
From chat to care
Choose one starting point. Staff can continue in your preferred language; response time varies.
Convenience channels
Use the channel that works best for appointment coordination and general questions.
Messaging is not monitored as an emergency service. Language availability and response times can vary.