Biocompatible silicone prosthesis that copies the relief of the endolarynx. This flexible mold supports the laryngeal framework in situations of organ trauma or after reconstructive surgery. Part of the Stening® laryngology line.
Product code: LP/LM/LG



Code LP/LM/LG
The Laryngeal Stent —also called laryngeal mold or laryngeal prosthesis— is a silicone prosthesis that copies the relief of the endolarynx. This flexible mold is an alternative to support the laryngeal framework in situations of organ trauma or after reconstructive surgery.
It has a very smooth surface and blunt edges that reduce trauma to the mucosa. Its flexibility favors tolerance, and its solid configuration prevents collapse and deformation. The Laryngeal Stent is radiopaque and comes with two curved silicone discs for external fixation.
Review the indications, available dimensions, how to use, care and warnings of the Laryngeal Stent.
The Laryngeal Stent is indicated to support the laryngeal framework and maintain the airway lumen in situations of trauma or reconstruction.
The Laryngeal Stent is offered in three sizes (small, medium and large). References A, B and C correspond to the dimensional diagram.

| Code | A | B | C |
|---|---|---|---|
| LP (Small) | 37 | 10 | 11 |
| LM (Medium) | 40 | 12 | 10 |
| LG (Large) | 47 | 15 | 16 |
Measurements expressed in millimeters, according to references A, B and C of the diagram. For specific sizing inquiries, contact us at (+54) 11 4553-5070 or (+54) 11 4551-2333.
The implantation of a laryngeal stent requires a prior tracheostomy, since oronasal breathing will not be possible.
The surgical procedure will be chosen by the treating physician, but in cases of stenosis an anterior and posterior laryngofissure with a costal cartilage graft is usually performed to achieve greater laryngeal stability. Once the stent is in the proper position, it can be fixed with two retention sutures running skin–subcutaneous tissue–stent–soft tissue–skin, and it will remain as a stent-tutor for as long as the physician deems necessary in each case. Removal is performed through the oral route, withdrawing it with forceps that grasp it by its upper end.
No additional care is required beyond the postoperative care of the laryngeal surgery.
The device must not be reused, as this could cause cross-contamination.
Contact us for personalized technical advice, sizing selection, custom manufacturing or international shipping inquiries.