
IBO prosthetic Screw, reference HEI-35201, M1.8 Fixation Screw HEI-35201. Used to fixate abutments, copings, multiunit components or impression copings to the matched implant fixture with controlled torque per the IBO loading protocol.
Used to fixate prosthetic components (abutments, copings, multiunit bases, impression copings) to the matched implant fixture or abutment platform. Final torque must be applied with the IBO torque wrench per the loading specification for the specific component and implant platform.
Platform pairing per the MFG# prefix — HEI for IBO Internal Hex platforms, HEC for Conical Reactive platforms (Ø3.0 / NP / RP / WP). Thread size per the M-designation in the product name.
| Manufacturer reference | HEI-35201 |
|---|---|
| Brand | IBO |
| Product family | Prosthetic / Fixation Screw |
| Designation | M1.8 Fixation Screw HEI-35201 |
| Drive interface | Per name — unigrip / hex / ACS 4-lobed |
| Material | Medical-grade Titanium alloy |
| Compatibility | Per MFG# prefix (HEI / HEC) and thread size |
| 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.