Confirme el dispositivo
Solicite el modelo exacto del sistema Ulthera y el aplicador planificado para cada área.
Confirme el modelo
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.
Respuesta directa
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.
Instrucciones oficiales de uso de Ultherapy PRIMEDo not transfer claims, images or protocols from Ultraformer MPT Program or legacy Ulthera SPT Program.
Solicite el modelo exacto del sistema Ulthera y el aplicador planificado para cada área.
Confirme el modeloSepare la flacidez cutánea, la posición del tejido, el volumen y la textura antes de discutir un plan de energía.
Mapee el áreaDiscuta dolor, enrojecimiento, hinchazón, moretones y los eventos menos comunes en las instrucciones oficiales, además de la ruta de escalación.
Solicite el plan de seguridadPatient 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.

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.
Utilice el canal que mejor funcione para la coordinación de citas y preguntas generales.
Messaging is not monitored as an emergency service. Language availability and response times can vary.