Technology
The Natural Choice
NaturalFit TR™ can be placed by both specialists and general dentists in one appointment, without drilling or multiple surgeries. This minimizes risk of damaging surrounding bone, tissue, and nerves.
Traditional Systems
Three-unit Bridge
A crown held in place by caps on the two adjacent teeth, which are filed down to hold it. The root is not replaced, so bone loss occurs over time.
Single Tooth Implant
A metal screw replaces the root through a multi-step surgical procedure that requires drilling, usually by a specialist over multiple visits and 6–9+ months.
Streamlined Clinical Procedure
Designed to reduce chair time and eliminate multi-stage surgical procedures.
No Capital Equipment Overhead
Requires no complex drill kits, specialized surgical guides, or extensive sizing inventory.
Anatomical & Aesthetic Match
Engineered from biocompatible white zirconia to support soft-tissue adaptation and eliminate dark metal margins.
Expanded Practice Capability
Allows general practitioners to offer advanced restorative solutions with confidence.
How It Works
01 Scan
Digital CBCT 3D scan and intraoral impression submitted electronically by the clinician.
02 Design
Proprietary software generates a 3D patient-specific root design matching natural socket geometry.
03 Produce
Device is precision laser-milled from high-purity zirconia and delivered sterile.
04 Place
Clinician inserts the anatomically matched device directly into the extraction socket.
Design
Screw-free
No unnecessary drilling, for self-guiding placement and optimized loading.
White zirconia
For natural aesthetics.
Micro-textured surface
Proprietary micro-texturing to support integration with bone.
Patient-specific root form
Maximizes bone contact for osseointegration and crown stability.
450+ patient cases reflect historical multi-center clinical evaluation studies conducted between 2013 and 2019
94.4%
survival, approx. 20 centers in 6 countries
96.6%
survival, Germany
90.0%
survival, U.S. study under IDE
Regulatory & Development Milestones
COMPLETE
Pre-clinical testing
COMPLETE
Manufacturer selection
Q4 2026 – Q2 2027
FDA 510(k) submission and review
Q1 2027
E.U. MDR registration
Q2 2027
FDA 510(k) clearance and commercial launch
Target dates are subject to regulatory review.