
IBO Open-Tray Impression Coping for conventional Impression workflows, reference HEC-43700, Open Tray Imp HEC-43700. Used to Transfer implant position from the patient's mouth to the laboratory stone model via a perforated (Open) Impression Tray, securing the Coping in place at the time of Impression material polymerization.
Used at the Impression visit in a conventional analog workflow. The Coping is screwed onto the implant connection, the Open-Tray Impression is taken, and the Coping is unscrewed through the Tray window before Tray removal — remaining captured in the Impression material so that the laboratory analog can be precisely seated at the Coping for a passive-fit master model.
Used with IBO implant platforms — Conical Reactive Ø3.0 / NP Ø3.5 / RP Ø4.3 / WP Ø5.0 series — and with multiunit abutment platforms (HE-48700 series). Confirm platform pairing via the MFG# prefix (HEI / HEC / HE) and the IBO catalogue cross-reference.
| Manufacturer reference | HEC-43700 |
|---|---|
| Brand | IBO |
| Product family | Open-Tray Impression Coping |
| Designation | Open Tray Imp HEC-43700 |
| Workflow | Conventional / analog Open-Tray pick-up Impression |
| Material | Ti-6Al-4V ELI Grade 5 |
| Includes | Captive fixation screw |
| Compatibility | IBO Conical Reactive + multiunit platforms — per MFG# prefix |
| 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.