# K113779: Conelog Implant System - Pathway: 510(k) (Traditional) - Applicant: Altatec GmbH - Decided: Dec 14, 2012 after 358 days - Product code: DZE (Implant, Endosseous, Root-Form) - Device class: 2 - Regulation: 21 CFR 872.3640 - Recalls of this device: none - Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026 ## Lineage Longest line of descent: 9 generations back to K925765 (1993). 126 ancestors in all. 14 later devices descend from it; 6 cite it directly. 0 of 141 devices in its family (counting itself) have a Class I recall. ## Predicates on the family tree (from the FDA summary) - K083496: Camlog Implant System Modified Implants and Abutments, Altatec GmbH (2009) Summary page 3. - K103252: Camlog Vario SR Abutments, Altatec GmbH (2011) Summary page 3. - K051636: Camlog Dental Implant Abutments, Healing Caps, and Accessories, Altatec GmbH (2006) Summary page 3. - K063779: Osseospeed 4.0S-6MM, Model 24619, Astra Tech, Inc. (2007) Summary page 3. - K011028: Screw-Vent Dental Implant System, Sulzer Dental, Inc. (2001) - K063341: 3I Osseotite Certain Dental Implants, Implant Innovations, Inc. (2007) Summary page 3. - K101849: Bicon Dental Implant System 3.0MM Bicon Dental Implant, Bicon, LLC (2010) Summary page 3. ## Most influential descendants - K193401: Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants (2020), 9 descendants of its own - K203252: Multi-unit Abutments for CONELOG (2021), 8 descendants of its own - K213106: BTI Interna Dental Implant System UnicCa - Prosthetic Components (2022), 3 descendants of its own - K240187: Tapered Pro Conical Implant System (2024), 2 descendants of its own - K231827: BTI Dental Implant System UnicCa® – Aesthetic Post Abutments (2023), 2 descendants of its own ## Indications for use CONELOG Implant System Implants are intended for immediate or delayed placement in the bone of the maxillary or mandibular arch. CONELOG Implant System Abutments are intended for use as support for crowns, bridges or overdentures. When a one-stage surgical approach is applied, the implant may be immediately loaded when good primary stability is achieved and the functional load is appropriate. CONELOG Implants with 3.3 mm diameter have the following additional specific indications: These are an alternative in cases where the alveolar ridge width is only 5 - 6 mm. Because of their lower mechanical strength compared with larger diameter implants, they should only be used under the following conditions: * As single implants, they should be used only to replace mandibular incisors and/or maxillary lateral incisors. * An edentulous arch can only be restored with a bar retained superstructure with at least four implants of 3.3 mm diameter without distal extensions. * Implants of 0 3.3 mm are suitable for a partially edentulous arch when combined with implants of larger diameter for splinted superstructures. However, the limited strength of the implants with 0 3.3 mm must be taken into account. * Avoid excessive mechanical stressing of the implants when using ball abutments in combination with 0 3.3 mm implants. * The healing time for 0 3.3 mm implants is at least 12 weeks. CONELOG Implants with 7 mm length have the following additional specific indications: CONELOG SCREW-LINE Implants should only be used when there is not enough space for a longer implant. Delayed loading in single tooth replacement is indicated with these implants. If the ratio of crown length to implant length is unfavorable the biomechanical risk factors have to be considered and appropriate measures have to be taken by the dental professional. CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch. CONELOG Vario SR components for crown and bridge restorations: Occlusal screw-retained crown, bridge and bar constructions on CONELOG implants in the anterior and posterior region of the maxilla and mandible CONELOG Vario SR components for bar restorations: Anchorage of implant-supported full dentures for the edentulous maxilla in conjunction with 4 or more CONELOG implants and in the edentulous mandible in conjunction with 2 or 4 or more CONELOG implants. Source page: https://510kreport.com/device/K113779 Methodology: https://510kreport.com/methodology