Profile: Invotec International Inc. markets products for head & neck surgery as well as facial plastic surgery. We supply disposable products to ear, nose and throat practitioners. We also deal in personal lighting system, sterilization trays, nasovisc & tracheostomy products. Our septal button reduces crusting, epistaxis and other symptoms of nasal perforations. Our bivalve fluoroplastic splint reduces or prevents adhesions between the septum and lateral nasal wall.

The company was founded in 1990, has revenues of USD 5-10 Million and is ISO 9001, ISO 9002, CE certified.

FDA Registration Number: 1052728

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• Reusable Hot /Cold Pack (FDA Code: IME / 890.5700) A cold pack is a device intended for medical purposes that consists of a compact fabric envelope containing a specially hydrated pliable silicate gel capable of forming to the contour of the body and that provides cold therapy for body surfaces.

• Single Use Surgical Instruments

• Sinus Endoscopy, Antrum Cannula

• Sinus Endoscopy, Nasal Scissors

• Sinus Suction Tips

• Sterile Surgical Drapes (FDA Code: KKX / 878.4370) A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination. The device includes a plastic wound protector that may adhere to the skin around a surgical incision or be placed in a wound to cover its exposed edges, and a latex drape with a self-retaining finger cot that is intended to allow repeated insertion of the surgeon's finger into the rectum during performance of a transurethral prostatectomy.

• Surgical Drapes (FDA Code: KKX / 878.4370)

• Surgical Drapes & Packs (FDA Code: KKX / 878.4370)

• Surgical Lighting

• Thermo Plastic External Nasal Splint

• Titanium Ossicular Replacement Prosthesis

• Tonsil Dissector (FDA Code: KBM / 874.4420)

• Tonsil Forceps

• Tonsil Grasping Forceps

• Total Ossicular Replacement Prosthesis (FDA Code: ETA / 874.3495) A total ossicular replacement prosthesis is a device intended to be implanted for the total functional reconstruction of the ossicular chain and facilitates the conduction of sound waves from the tympanic membrance to the inner ear. The device is made of materials such as polytetrafluoroethylene, polytetrafluoroethylene with vitreous carbon fibers composite, porous polyethylene, or from a combination of these materials.

• Total Replacement Titanium Middle Ear Implants

• Tracheal Tube with/without Connector (FDA Code: BTR / 868.5730) A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.

• Tympanostomy Tube (FDA Code: ETD / 874.3880) A tympanostomy tube is a device that is intended to be implanted for ventilation or drainage of the middle ear. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. A type of tympanostomy tube known as the malleous clip tube attaches to the malleous to provide middle ear ventilation. The device is made of materials such as polytetrafluoroethylene, polyethylene, silicon elastomer, or porous polyethylene.

• Urology Surgical Drapes (FDA Code: KKX / 878.4370)

• Y-Stent Forceps