What is it?
The device has a specified polymer, absorption profile, surface or suspension design, length and sterile delivery system; different threads are not interchangeable.
Thread Lift · Aesthetic Medicine · Istanbul
Thread Lift · Aesthetic Medicine · Istanbul
A thread lift is not one device. Polydioxanone, poly-L-lactic-acid, polycaprolactone or other materials; smooth, barbed or cone designs; absorbable or non-absorbable systems; and different tissue paths have different aims and risks.
Thread placement is not equivalent to a surgical facelift. Degree, symmetry and duration of change cannot be guaranteed, and visible, palpable or extruded threads may require further treatment.
Quick Orientation
Identity · composition · preparation · route
A responsible discussion identifies the exact preparation or device, how it was made, where it is intended to act and which clinical question is being assessed.
The device has a specified polymer, absorption profile, surface or suspension design, length and sterile delivery system; different threads are not interchangeable.
Polymer manufacture, thread geometry, barbs or cones, needle or cannula assembly, sterilisation, packaging, expiry and device status define the implant.
The thread passes through a planned soft-tissue plane to provide limited mechanical support. Incorrect depth or path can injure or distort tissue.
A limited contour or tissue-support aim is assessed and kept separate from volume replacement, skin-quality treatment and surgical lifting.
What is Thread Lift?
An implanted medical device with material and design variables
The intended role, product identity and target tissue stay visible so unlike procedures are not presented as one interchangeable class.
What Thread Lift can do
What Thread Lift cannot do
If the device, tissue plane, realistic mechanical aim or management of a visible, infected or extruded thread is unclear, implantation should not proceed.
Medical Suitability
Clinical question before method selection
Tissue weight, skin quality, facial movement, asymmetry, scars, prior fillers or surgery, neurological and vascular anatomy and surgical alternatives are reviewed.
Limited support or contour is distinguished from volume loss, skin texture and surgical-level laxity.
Skin thickness, fat compartments, ligament support, asymmetry and dynamic facial movement affect suitability.
Vessels, nerves, glands, scars, previous surgery, filler and earlier threads alter the risk.
Material, design, absorption profile, sterile system, manufacturer and authorised use are checked.
When tissue excess or displacement exceeds a limited thread aim, surgical review or no treatment may be more honest.
Product and Treatment Path
Traceability without a public injection recipe
A thread is not selected by brand familiarity alone. Mechanical aim, tissue thickness, sterile device and anatomical limits remain connected.
The exact polymer, surface design, anchoring concept, absorption profile and sterile delivery system are identified.
The planned support task is matched to soft tissue and movement without publishing vectors or entry points.
Early symmetry and skin condition are followed by later review for visibility, migration or extrusion.
No material selection, thread number, vector, entry point, tissue path, depth, needle/cannula, anchoring or tension protocol is provided publicly.
Evidence and Limits
Read the data at product and indication level
Published series use different polymers, designs, combinations, grading methods and follow-up. Many do not provide a direct comparison with surgery or no treatment.
Findings from one polymer and design cannot be transferred to another suspension or volumising thread.
Studies combining filler and threads cannot establish the independent contribution of each treatment.
Small retrospective or single-centre studies do not create a personal persistence guarantee.
Dimpling, asymmetry, infection, visibility, extrusion and anatomical injury require longer follow-up than an early photo.
Current evidence does not establish equivalence to facelift surgery, one best thread, predictable duration or freedom from delayed device problems.
Individual Plan
One indication · one traceable intervention · one review point
Tissue diagnosis, limited mechanical aim, exact device, surgical alternative, early wound review and delayed stop criteria are documented.
The desired change is compared with tissue weight and surgical-level laxity before a thread is selected.
Polymer, design, sterile system, expiry and authorised use remain traceable.
Baseline differences and movement are documented so early swelling is not mistaken for device failure.
Infection, extrusion, persistent dimpling or anatomical injury may require intervention or surgical review.
Course and Follow-Up
Expected reaction · adverse effect · clinical endpoint
Bruising, tenderness and temporary dimpling can occur, but persistent distortion, visibility, infection or extrusion must not be normalised.
Material, design, batch or lot, region and baseline asymmetry remain traceable.
Increasing pain, blanching, heat, discharge, weakness or marked asymmetry needs prompt assessment.
Persistent dimpling, palpability, migration or extrusion is assessed after early swelling changes.
Infection, anatomical injury, unacceptable distortion or no meaningful support prevents routine addition of threads.
Risks and Alternatives
Material, anatomy and route shape risk
Procedure risk includes both early wound events and delayed problems related to position, material and tissue response.
Active infection, inflamed skin or unexplained painful pre-existing threads argue against an immediate procedure.
Placement that is too superficial, the wrong vector or excessive pull can promote dimpling, visibility and asymmetry.
Severe increasing pain, pallor, dark skin, rapidly growing swelling or new facial weakness is urgent.
Fever, pus, increasing redness, an open entry point or a visible thread require personal examination.
Severe pain, blanching, fever, discharge, thread extrusion, new facial weakness or rapidly worsening asymmetry requires prompt local medical assessment. Alternatives may include observation, filler for a separate volume indication, device-based treatment, surgical lifting or no treatment.
Istanbul and Follow-Up
A treatment decision must remain reviewable after travel
International care is not reduced to a treatment day. The in-person examination, exact intervention, early review and later endpoint are connected before departure.
History, previous procedures and the specific thread lift question prepare the visit without confirming suitability.
Anatomy, tissue, active disease, product or device status, risks and alternatives are reviewed together.
Product or device identity, batch where relevant, treated region, route and observations remain traceable.
Expected reactions, stop criteria, local medical access and the later clinical endpoint are agreed before return travel.
The Doctor Aslan Approach

Product-specific, anatomy-led and reversible in decision-making
Material, design, tissue path and limited mechanical objective are explained without promising a facelift result or fixed persistence.
Threads do not reproduce surgical dissection, tissue removal or fixation.
Polymer, design, sterile system and absorption profile stay visible.
Tissue weight, asymmetry and dynamic anatomy guide suitability.
Visibility, dimpling, infection and extrusion have a clear review route.
Frequently Asked Questions
Short and clear
These answers provide general orientation and do not replace personal diagnosis or treatment planning.
Smooth mono or screw threads do not have a comparable holding system for targeted tissue repositioning. Depending on the product, lifting threads use barbs, cones or defined anchoring. Materials such as PDO, PLLA or PCL, thread length, thickness, degradation and intended use also differ. The word ‘thread’ therefore does not make the procedures interchangeable.
No. A thread lift does not remove excess skin and cannot provide the same surgical exposure and tissue repositioning. In a suitable starting situation it may support a limited contour change. Duration and extent depend on tissue, product, design, vector, technique and time course. Studies also show satisfaction may decline over longer follow-up; fixed persistence cannot be promised.
No. Absorbable means the material degrades over a product-specific period; it cannot be dissolved at the push of a button. A thread may integrate into tissue, move, become visible or palpable, extrude or cause inflammation. Whether observation, correction or removal is appropriate and possible depends on material, position, symptoms and time course.
Severe or increasing pain, white, grey or dark skin, rapidly growing one-sided swelling, persistent bleeding, new numbness or facial weakness require immediate local assessment. Fever, pus, increasing redness and heat, an open entry point, or a visible or extruding thread must also not wait for a later online reply.
Next Step
Define the mechanical aim · verify the thread · compare surgery