Uneva+ The implant with external connection

Uneva+ implants are placed in 2-stage surgery based on the latest scientific data acquired in implantology to limit any marginal bone loss and optimise the primary anchorage. Its external hexagonal connection is Branemark RP-compatible on Ø 3.6-4.1 implants . This therefore provides you with numerous interchangeabilities with parts from the abovementioned brand.

Indications

• Versatile implant.
• Suitable for high bone densities.

This kit includes all the instruments necessary for carrying out the surgical protocol and the management of all bone densities for all lengths and all diameters of Uneva+ implants.

Reduced format for increased space in the sterile field and the autoclave.

Readability of sequences due to the presentation of the instruments in order of use and the protocol table.

Colour coding of plugs and stiffeners according to implant diameter.

External hexagonal connection

Compatible with Bränemark MK III and MK VI

  • This connection is available on implants Ø 3.6 and Ø 4.1.

Prosthetic shoulder on implants Ø 4.8

  • Increase in the height of the connection and engagement of the post to give it greater stability.
  • Better distribution of constraints.
  • Centring of the prosthetic part.
  • Guaranteed impermeability of the prosthetic seal.

Microthread synchronous with the macrothread

  • Insertion without tearing the cortical bone.
  • Stabilisation of the cortical bone by micro-stimulation.
  • Optimised primary anchorage.

Double asymmetrical thread

  • Homogeneous distribution of masticatory forces.
  • Excellent primary stability immediately after implant placement.
  • Decreased heating of the bone and insertion time.

Central protusion between threads

  • Contact surface with bone tissue increased by 15%.
  • Facilitates osteogenesis.
  • Activates cell reconstruction.

Engaging atraumatic apex

  • Vent closer to the apex to improve the self-tapping effect of the spirals.
  • Threading from apex for greater self-tapping capacity of the implant and improved apical fixation.
  • Safe to use in the sinus floor region.

Proven STAE® surface condition

  • Titanium oxide micro-sanding.
  • Etching with nitric and hydrofluoric acids.
  • 23 years of clinical experience.

Direct mandrel implant driver

  • Time saved during surgery.
  • Better visibility of the placement level and the orientation of the connection.
  • Gingival height provided.