Abstract: PROCEDURE FOR THE INDIVIDUAL TRACEABILITY OF DENTAL IMPLANT PARTS AND UNITARY IDENTIFICATION SYSTEM FOR IMPLEMENTING THIS PROCEDURE that comprises: the association of each part (1), which is manufactured with a single identification code (2); the incorporation of that code (2) into the individual packaging (3) in which the part (1) is distributed and marketed, recorded on a radio frequency label (5) and/or printed on an adhesive label (6); and the implementation of specific management software in a website (4) on the Internet that associated the code (2) with traceability information of each specific part (1), associates implants with accessories and provides a user with access to it in that website (4). The unitary identification system consists of a code (2) that is unique and different for each part (1), which is a numerical code, and the specific management software that associates each code (2) with the traceability information of each part (1).

Abstract: PROCEDURE FOR THE INDIVIDUAL TRACEABILITY OF DENTAL IMPLANT PARTS AND UNITARY IDENTIFICATION SYSTEM FOR IMPLEMENTING THIS PROCEDURE that comprises: the association of each part (1), which is manufactured with a single identification code (2); the incorporation of that code (2) into the individual packaging (3) in which the part (1) is distributed and marketed, recorded on a radio frequency label (5) and/or printed on an adhesive label (6); and the implementation of specific management software in a website (4) on the Internet that associated the code (2) with traceability information of each specific part (1), associates implants with accessories and provides a user with access to it in that website (4). The unitary identification system consists of a code (2) that is unique and different for each part (1), which is a numerical code, and the specific management software that associates each code (2) with the traceability information of each part (1).

Abstract: PROCEDURE FOR PRODUCING IMPLANTS WITH A PERSONALISED SURFACE that involves the cleaning/activation of the implant surface by means of plasma technology using oxygen or argon plasma to obtain surfaces with no organic compounds or oxide layers, and the application of a liquid solution that is designed for each patient and contains a single osteoconductive, osteoinductive, antibiotic, antibacterial or probiotic component, or a combination of any of them. The cleaning/activation of the implant surface by means of plasma technology may be carried out in the clinic or in the implant production plant and the liquid solution may be applied in the dental clinic just before the implant placement procedure.

Abstract: An osteotomy marker (1) comprised of an interchangeable head (3) connected to a guide wire (2), so that the guide wire (2) is fixed to a surgical hand piece (15) and the interchangeable head (3) establishes a predetermined distance (D) with respect to a reference point at which that interchangeable head (3) guides a cutting tool (16) that performs the osteotomy; the interchangeable head (3) is formed by a central body (9) to which are joined a connector (5) and a support element (11) with a main body (28) that has two flat sides (29a, 29b) parallel to each other, establishing the predetermined distance (D) between the first flat side (29a) and a groove (10) in the central body (9), with the support element (11) resting on the first flat side (29a) at the reference point and the groove (10) marking the position and the predetermined distance (D) for performing the osteotomy.

Abstract: An alveolar ridge distractor for distracting a bone fragment (2) with respect to a maxillary bone (1) separated by an osteotomy line (11); the distractor is comprised of a threaded rod (5) with an upper piece (3) and a lower piece (4). The threaded rod (5) is formed by a top part (7) where the thread has a specific rotation direction and a bottom part (8) where the rotation direction of the thread is opposite to that of the top part of the rod (7); the upper piece (3) is located at the top of the rod (7) and the lower piece (4) is located at the bottom part of the rod (8); both bodies (3 and 4) have an end part (16) with no external thread, generating a free ring (12) in the area in which both bodies are joined, with no thread. That free ring (12) which is not threaded, is positioned to coincide with the osteotomy line (11).