DURA-VIT 3P
DURA-VIT 3P

Dura-Vit 3P

The DURA-VIT 3P implant is suitable for all surgical procedures and excellent in all bone types, and thanks to its characteristics it guarantees better control during implant placement and high primary stability.

PROPERTIES
  • Excellent in all bone types (especially D1-D2). 
  • Ensure high primary stability. 
  • Ideal in sites next to sinus or nerve.
  • Suitable for all surgical procedures.
  • Grade 4 Titanium.
SIZES
  • 5/14 – 5/12 – 5/10 – 5/8 – 5/6.5
  • 4.5/14 – 4.5/12 – 4.5/10 – 4.5/8
  • 4/14 – 4/12 – 4/10 – 4/8 – 4/6.5
  • 3.5/14 – 3.5/12 – 3.5/10 – 3.5/8
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Description

DIAMETERS & LENGTHS

The color code of the implant diameters allows an intuitive selection of the surgical instruments; just pick them until you reach the instrument of the color of the internal vial containing the implant to be placed.

The 3P line is available in 4 diameters (3.5 – 4.0 – 4.5 – 5.0 mm) and in 5 lengths (6.5 – 8.0 – 10-12-14 mm).

All sizes have a single CONEXA connection. Inside the surgical instrumentation there are the instruments (drills, compactors and countersinks) for the correct preparation of the implant sites and the stops that guide the instruments to the right preparation depth. Discover the kits and their components!

SURGICAL TECHNIQUE

Take a look at all the uses of the 3P line, the surgical technique, the instruments and the prosthetic solutions to be applied to the line.
A single connection common to the 3P, EV, WIDE and PTERYGO lines to facilitate management and choice from a wide range of abutments, attachments and posts.

A UNIQUE PACKAGING

The implants are equipped with a new functional and safe packaging thanks to the anti-tamper opening. The implant-holder ampoule keeps the implant in position, ready to be taken with the use of ratchet or contra-angle wrenches. Inside the package of each implant there is a healing screw and a closing cap. A package designed to ensure the sterility of the product and to contain the implant in a practical and safe way accompanied by a healing screw and a transmucosal screw. In each package there are instructions for use, labels to be used to update the clinical report and to be affixed to the implant passport supplied.

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