IBO contra-angle Implant Driver designed for use with a contra-angle surgical handpiece during Implant placement and prosthetic seating. Reference ACTL, Contraangle Long Implant ACTL, allows controlled motorized rotation under the practitioner's direct control.
Used at the Implant placement stage with a contra-angle surgical handpiece operating within the manufacturer's recommended rotational speed and torque envelope. Final placement torque must be verified and finalized with the IBO ratchet wrench per the loading protocol.
Compatible with IBO Conical REACTIVE platforms via matched Driver tips. Used with standard latch-type contra-angle surgical handpieces (ISO 1797-1 dimensional interface). Consult the IBO surgical kit reference for specific platform-to-Driver pairings.
| Manufacturer reference | ACTL |
|---|---|
| Brand | IBO |
| Product family | Contra-Angle Implant Driver |
| Designation | Contraangle Long Implant ACTL |
| Shank type | Latch-type (ISO 1797 contra-angle) |
| Material | Surgical titanium alloy / Stainless Steel |
| Reusable | Yes — autoclave-compatible per IFU |
| Compatibility | IBO Conical REACTIVE platforms · latch-type surgical handpieces |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
Machined from medical-grade Ti-6Al-4V ELI titanium (Grade 5), ASTM F136 / ISO 5832-3, selected for biocompatibility, mechanical strength and chemical stability in the oral environment.
All materials and processes comply with current regulations and are subject to full traceability from raw material to final validation.
Supplied in the manufacturer's validated condition for clinical use. Follow the package insert and IBO Instructions for Use for handling, storage and any chairside preparation steps. Do not modify the geometry or surface in any way; doing so compromises both clinical fit and regulatory clearance.
Single-use device. Single patient, single procedure. Discard unused components per local biohazard regulations.
IBO operates under ISO 13485:2016 quality management for the manufacturing of medical devices, holds the AEMPS Spanish Agency of Medicines and Medical Devices licence, and every IBO component carries the CE marking MDR, assessed by a Notified Body.