IDL Dental Technologies manufactures a complete range of dental implant systems designed for the demanding clinical workflows of modern implantology. Our platform is built on three engineering principles that apply to every implant in our portfolio.
Grand Morse 16° conical connection serves all implant diameters with a single prosthetic platform — one set of abutments, healing caps, and impression copings across the entire range. Hydrophilic RBM surface treatment accelerates osseointegration in the critical first hours after placement. Commercially pure titanium Grade 4, manufactured per ASTM F67, provides biocompatibility without aluminum or vanadium exposure to peri-implant tissues.
From standard tapered placements to zygomatic fixation in severely atrophic maxilla, every implant uses the same prosthetic components — simplifying inventory for clinics and laboratories while reducing the risk of prosthetic errors.
Universal tapered implant for two-stage and immediate protocols.
Progressive threads adapt to all bone densities from D1 to D4.
Anchorage in the zygomatic bone for severe maxillary atrophy.
Full-arch rehabilitation without bone grafting or sinus lifting.
Monolithic single-body design. No abutment screw, no micro-gap.
Ideal for narrow alveolar ridges and flapless protocols.
Monolithic design with bendable neck up to 45°. Self-condensing threads for primary stability in soft bone (D3–D4).
Fixed-neck monolithic design for maximum rigidity. Compressive threads condense bone for immediate stability.
IDL implants are not a collection of independent products — they are components of a single prosthetic and surgical system. Every fixture, abutment, healing cap, impression coping, and analog is engineered to function together.
Surgical drills align with implant geometries. Prosthetic components snap onto the same Grand Morse 16° taper regardless of which implant line is used. This is a design principle applied at every stage of manufacturing. From the first CNC cut of the titanium blank to the final sterilization cycle, every component is validated against the tolerances of the neighboring parts in the system.
For the clinician, this means predictable workflows: no adapters, no third-party compatibility checks, no mixing and matching. For the laboratory, it means simplified inventory and reduced error rates. For the patient, it means a restoration that performs as a cohesive biomechanical unit for the lifetime of the implant.
All components are manufactured in Israel under ISO 9001:2015 and ISO 13485:2016 certified quality systems. CE-marked under the Medical Device Regulation (MDR). FDA 510(k) submission in process. Trusted by dental professionals in 30+ countries worldwide.
All IDL dental implants are manufactured from commercially pure titanium Grade 4 in accordance with ASTM F67 — the international standard for unalloyed titanium surgical implants. Grade 4 titanium provides the optimal combination of mechanical strength and biological response for long-term intraoral use, without the aluminum and vanadium content of Ti-6Al-4V alloys.
Surface treatment is applied in IDL's Israel manufacturing facility under controlled conditions, with each production batch undergoing surface topography verification, cleanliness testing, and sterilization validation. Final products are delivered sterile, individually packaged, with lot traceability to the original titanium stock.
One Grand Morse 16° connection for all implant diameters. Simplified inventory, zero compatibility issues across the product line.
Hydrophilic RBM surface accelerates bone-to-implant contact in the first 24-48 hours after placement, supporting immediate loading protocols.
Commercially pure titanium per ASTM F67. No aluminum or vanadium exposure to peri-implant tissues.
CE-marked under MDR. ISO 9001:2015 and ISO 13485:2016 manufacturing. Traceability for every production batch.
