Directorio Program

Programs para las preguntas que la gente hace más frecuentemente.

Start with a Program or with the concern you notice. Each page brings together a direct answer, recovery questions, suitability limits and a clear consultation path.

Iniciar consulta Preocupaciones

Choose a Program to review general information, recovery questions, suitability limits and the next consultation step.

Programs para las preguntas que la gente hace más frecuentemente.

Elige un Program para revisar información general, preguntas sobre recuperación y el siguiente paso de la consulta.

Planificación clara de precios: Revise los precios publicados o solicite una cotización detallada antes de decidir.
Pacientes de 50+ países: Información de citas internacionales con cuatro recorridos web compatibles.
Bangkok central: Siam Square One, conectado a BTS Siam Salida 3.

Retrato editorial que representa una Ruby No.5 consulta

Ruby No.5 Thread Lift Program

A consultation-led thread Program described by Waleerat as a subtle skin-quality option. A physician must assess whether it fits your anatomy, goals and timing.

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Retrato editorial de piel para el Emerald Program

Emerald Lower-Face Thread Lift Program

Waleerat describes Emerald as a thread-based Program intended to support the lower face and jawline with absorbable synthetic molding-cog threads. It is not a universal answer for facial laxity: the thread plan, likely change, limitations and recovery need an in-person physician assessment.

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Retrato editorial de la zona ocular para el Pailin Program

Pailin Eye Thread Lift Program

Waleerat identifies Pailin as a PDO cog-thread Program for the eye-area lifting conversation. The eye and brow-tail area requires individual anatomical assessment; a physician must decide whether threads, another approach or no procedure is appropriate.

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Perfil facial editorial para el levantamiento con hilos nasal Program

Nose Thread Lift Program

Waleerat describes the Nose Thread Lift Program as a thread-based option for selected questions about nose-bridge structure. It uses absorbable synthetic threads, but the number, placement, likely change and suitability depend on anatomy and previous procedures assessed by a physician.

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Retrato editorial de piel que introduce información sobre levantamiento con hilos Program dirigido a la preocupación

Thread Lift Program

Temporary swelling, bruising, tenderness, tightness or asymmetry can occur. Less-common complications need prompt clinical review. A Program is commonly planned as one treatment followed by review, but there is no fixed session count for everyone: anatomy, material, goal, previous procedures and recovery determine the plan.

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Sala de tratamiento Waleerat Clinic para XERF Program orientación de decisión

XERF Program

People asking about facial firmness or an energy-based, non-surgical option may use this guide to prepare questions. Suitability is not established online. Confirm health history, previous energy treatments or implants, treatment area, applicator, shot and energy context, comfort plan, traceable record, aftercare, follow-up and the current itemised price.

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Sala Waleerat Clinic introduciendo comparación de Ultraformer MPT Program centrada en la preocupación

Ultraformer MPT Program

The conversation may begin with a soft jawline, lower-face laxity, under-chin or neck concerns, or reduced skin firmness. These are not interchangeable. A physician assesses whether the concern is primarily skin, tissue position, fat, muscle or structure before selecting a device, depth or shot plan.

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Sala de tratamiento de Waleerat Clinic para la guía de decisión del Oligio Program original

Oligio Program

No. Oligio Program on this page refers to the original model from South Korean manufacturer WONTECH. Manufacturer and FDA records describe it as a 6.78 MHz monopolar radiofrequency system that delivers energy through a disposable tip while conductively cooling the epidermis. Oligio X Program is a separate later model in the same lineup. The clinic should confirm the exact device, tip, treatment area, settings context and follow-up in writing before treatment.

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Waleerat Clinic sala de tratamiento para una Oligio X Program guía de decisión

Oligio X Program — Korean Monopolar RF Program

Oligio X Program uses a separate later model from South Korean manufacturer WONTECH. The manufacturer describes GXG dual-mode delivery and an updated cooling workflow, while FDA records describe the same 6.78 MHz monopolar-radiofrequency principle as the original Oligio Program. A newer model is not automatically the right plan: the physician must confirm the concern, anatomy, previous procedures, implanted devices, treatment map, tip and settings context.

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Sala de Waleerat Clinic presentando el dispositivo Ultherapy PRIME Program e información de consulta

Ultherapy PRIME Program

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.

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Retrato editorial de la piel para el TheraFill Program

TheraFill Atelocollagen Program

Waleerat describes TheraFill as an injectable porcine-derived atelocollagen Program for selected under-eye, deeper-fold or skin-quality concerns. It is not a thread lift and it is not halal-compatible. A physician assessment is required to discuss allergy history, suitability and alternatives.

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Mujer en la sala de tratamiento del Waleerat Clinic para información de consulta de Ultracol Program

Ultracol Program

Ultracol Program is a medical-device product based on biodegradable PDO (polydioxanone) microspheres. The manufacturer's current public information describes a Korea MFDS-approved indication for temporary improvement of bilateral nasolabial folds. The exact product variant, planned area, amount and local product documentation used at Waleerat Clinic must be verified during consultation. Ultracol Program is not PDRN, salmon-derived material or an HA filler.

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Botox Program

Price cannot be interpreted without the brand and basis. The treatment area describes where the concern is; units describe the dose selected after assessing muscle activity, anatomy, previous toxin and goal. Use the published 100-Unit prices for like-for-like comparison, then obtain a physician-confirmed area and unit plan before booking treatment.

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HA Filler Program

Compare the exact product, amount in cc, treatment area, physician assessment, lot traceability, aftercare and follow-up on the same basis. Restylane and Juvéderm are product families rather than one interchangeable item. A physician must assess anatomy, previous filler, medical history, alternatives and vascular risk before recommending any area or amount.

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Sculptra Program

Sculptra Program uses poly-L-lactic acid (PLLA) as a collagen-stimulating injectable. It does not work like an HA gel placed for immediate volume shaping, and change develops gradually. Suitability, vial and session planning, preparation, aftercare and follow-up must be confirmed after a physician assessment.

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Rejuran Program

The manufacturer lists Rejuran Program as a PN (polynucleotide) medical device intended for temporary improvement of facial wrinkles. Product variants and intended areas differ. A physician should verify the exact product, local indication, treatment area, technique, medical history, session plan, risks, aftercare and follow-up before recommending treatment.

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Pico Laser Program

Medical lasers use focused light. A Pico Laser Program should therefore be discussed by the actual concern, skin type, pigment depth, area, exact device and wavelength—not by the word ‘pico’ alone. FDA patient guidance notes possible risks including incomplete treatment, pain, infection, bleeding, scarring and skin-colour change. Suitability, settings, session plan and aftercare require clinical assessment.

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Juvelook Program

Official product materials identify Juvelook Program as PDLLA-based. That identifies a product characteristic, not individual suitability or a universal protocol. A physician should verify the exact product and packaging, locally applicable indication, treatment area, preparation, technique, session plan, risks, recovery, aftercare, follow-up and current itemised quotation before treatment.

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Radiesse Plus Program

FDA device records describe Radiesse Program as an injectable implant containing calcium hydroxylapatite (CaHA) microspheres in a gel carrier, and the Radiesse Program (+) supplement records the addition of lidocaine. Product identity does not determine whether it is appropriate for a person, area or goal. A physician must review medical history, exact product, locally applicable indication, treatment area, amount, technique, risks, aftercare, follow-up and alternatives before treatment.

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Laser Hair Removal Program

Start with skin tone, hair colour and thickness, treatment area, recent sun exposure, medicines and previous reactions. Ask which device and wavelength will be used, who assesses the settings, how sessions are spaced, what aftercare applies and how the current price is calculated. Long-term reduction usually needs a course rather than one session, but the plan varies.

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Profhilo Bio-Remodelling Program

The official instructions include a 2 mL configuration containing 32 mg high-molecular-weight and 32 mg low-molecular-weight hyaluronic-acid sodium salt. They describe an initial cycle of two sessions 30 days apart, with later maintenance individualized. This is product guidance, not confirmation of the clinic's exact pack or an automatic plan for every patient or area; a physician must verify the product, suitability, local use, risks and alternatives.

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Nucleofill Program

The official manufacturer describes Nucleofill as a range of highly purified, high-viscosity polynucleotide-based biostimulating gels, with products and concentrations varying across the range. A category claim cannot identify the exact variant or personal plan. The physician must confirm product, packaging, concentration, area, sessions, risks, aftercare and alternatives.

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Oligio Program vs Oligio X Program

Both use 6.78 MHz monopolar radiofrequency, but they are separate device models with separate FDA records. The original Oligio Program record describes energy delivery through a disposable tip with conductive epidermal cooling. Oligio X Program is a later model; the manufacturer describes GXG dual-mode delivery and an updated cooling workflow. These differences do not prove that one model is universally better. Confirm the exact model, tip, area, treatment map, settings context, aftercare and follow-up in writing.

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Juvelook Program vs Rejuran Program

Official product materials identify Juvelook Program as PDLLA-based, while PharmaResearch lists Rejuran Program with PN (polynucleotide) composition. That difference means there is no universal ‘better’ option. A physician must verify the exact product and variant, locally applicable indication, treatment area, technique, session plan, risks, recovery and alternatives for the concern being assessed.

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Láser Labial Program vs Tatuaje Labial Program

A laser procedure uses focused light to target selected tissue or pigment, while lip tattoo or permanent makeup introduces pigment into skin with needles. Neither automatically treats the cause of a colour change, and neither can promise permanently pink lips. Compare assessment, goal, permanence, colour change over time, pain control, infection or scarring risk, recovery, aftercare and future correction or removal before deciding.

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Radiesse Program vs Sculptra Program

FDA records identify Radiesse Program as CaHA microspheres in a gel carrier and document the addition of lidocaine for Radiesse Program (+), while official Sculptra Program information identifies an injectable based on poly-L-lactic acid (PLLA). Material identity alone does not decide which, if either, is suitable. The exact product, locally applicable indication, anatomy, area, desired timing, amount or vial basis, sessions, injection technique, risks, aftercare and alternatives require physician assessment.

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