Human sinus elevator Intralift™

piezoelectricapplications

Product overview
The Intralift kit is designed for internal (crestal) sinus lift procedures using an ultrasonic system. It enables a controlled, minimally invasive membrane elevation sequence with dedicated TKW tips.

Clinical application
Intended for internal sinus lift via the crestal approach. Membrane elevation is performed by hydrodynamic pressure using the non-cutting TKW5. Use with a compatible ultrasonic device and frequency modulation to reduce membrane stress. Avoid direct vibrating contact of TKW5 with the membrane.

Components

• TKW1: conical diamond-coated tip for pilot drilling of dense cortical bone to the sinus floor.
• TKW2: cylindrical diamond-coated tip for penetration through the sinus floor.
• TKW3: cylindrical diamond-coated tip for progressive enlargement of the access canal to the membrane.
• TKW4: cylindrical diamond-coated tip for preparing the bony receptacle and widening the access canal.
• TKW5: non-cutting tip for membrane detachment by hydrodynamic pressure. Do not place TKW5 in vibrating contact directly on the membrane.

Key features

• Membrane elevation via hydrodynamic pressure (TKW5)
• Ultrasonic frequency modulation to limit membrane damage risk
• Cavitation effect for improved visibility of the surgical field
• Diamond-coated tips with increasing diameters (1.35 mm to 2.80 mm) for progressive access
• Compatible with ultrasonic surgical units supporting frequency modulation

Multimedia
Available educational resources: Intralift 3D video and technique video for TKW1.

Regulatory information
Class I medical device – CE. This medical device is not reimbursed by health insurance organizations. Read the labeling and instructions before use. Manufacturer: SATELEC® (FRANCE).

Technical specifications

• Intended procedure: Internal sinus lift (crestal approach)
• Primary elevation instrument: TKW5 (hydrodynamic pressure)
• Complementary tips included: TKW1, TKW2, TKW3, TKW4
• Tip diameters: 1.35 mm to 2.80 mm (progressive sequence)
• Technology: Ultrasonic frequency modulation and cavitation effect
• Regulatory status: Class I medical device – CE
• Manufacturer: SATELEC® (FRANCE)