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Anterior restorations (Class III, IV) Class V restorations (cervical caries, root erosion, wedge-shaped defects) Restorations in the posterior region (Class I and II) Veneering of discolored anterior teeth Splinting of mobile teeth Repair of composite and ceramic veneers

Device Description

Light Cure Composite is a state-of-the-art light-curing, radiopaque, nano-hybrid composite for the restorative therapy. The device cures with light at the wavelength range of 400–500 nm (blue light). The device is paste contained in PP syringe.

AI/ML Overview

Here's an analysis of the provided text regarding the acceptance criteria and study for the device:

1. Table of Acceptance Criteria and Reported Device Performance

Test Item	Acceptance Criteria	Reported Device Performance
Outward appearance-ISO 4049	According to visual inspection, the product should be uniform in texture and should be a paste without visible impurities and foreign matter.	Meet the requirement
Sensitivity to ambient light-ISO 4049	The material of sample remains physically homogeneous.	Meet the requirement
Depth of Cure-ISO 4049	≥1.5mm	≥1.5mm
Flexural strength-ISO 4049	≥80Mpa	≥80Mpa
Water sorption-ISO 4049	≤40µg/mm³	≤40µg/mm³
solubility-ISO 4049	≤7.5µg/mm³	≤7.5µg/mm³
Shade-ISO 4049	Without the need for a magnifying glass to observe with the naked eye, the cured material should be evenly colored.	Meet the requirement
Color comparison for color stability-ISO 4049	Only slight changes are allowed.	Meet the requirement
Appearance of container-ISO 4049	Visually observe that the surface of the container should be smooth, without scratches, cracks, burrs, small notches or macroscopic defects caused by mechanical processing.	Meet the requirement
Delivery performance of container-ISO 4049	Remove the syringe cap and turn the container push rod clockwise allowing resin to be smoothly squeezed out of the syringe without obstruction.	Meet the requirement
Compressive Strength	≥ 200 Mpa	Meet the requirement (Mean: 286.5)
Elastic Modulus	≥ 6 Gpa	Meet the requirement (Mean: 8.5)
Surface Hardness	≥ 60 (HV)	Meet the requirement (Mean: 63.1)
Particle size	0.4-2μm	(Value not explicitly stated as "meet requirement," but compared in section 6 as 0.4-2μm)
Radio-opacity	Mean: 2.27mm (This value is provided as a characteristic, not an acceptance criterion with a pass/fail. However, it is explicitly listed as a 'target' value.)	Mean: 2.27mm
Biocompatibility	Meet ISO 10993-1 - Biological evaluation of medical devices — Part 1: Evaluation and testing.	Meet ISO 10993-1

2. Sample Size Used for the Test Set and Data Provenance

The provided document does not explicitly state the sample sizes used for each specific test in the "Non-clinical performance Data" section. It lists performance results but not the number of units tested.

The data provenance is from non-clinical performance testing, likely conducted by the manufacturer, Sincera Technology (Changchun) Co., Ltd. The country of origin for the testing would be P.R. China, based on the submitter's address. The data is prospective in the sense that it was generated for the purpose of demonstrating the device's performance against established standards.

3. Number of Experts Used to Establish Ground Truth for the Test Set and Their Qualifications

This document describes a non-clinical performance study of a dental material, not a diagnostic device requiring human interpretation of images or clinical data. Therefore, there is no mention of "experts" or "ground truth" in the context of clinical interpretation for a test set. The "ground truth" for these tests is implicitly defined by the ISO standards themselves, which specify measurement methodologies and acceptance criteria.

4. Adjudication Method for the Test Set

As this is a non-clinical performance study against ISO standards, no adjudication method (like 2+1 or 3+1) is applicable or mentioned. The results are based on direct measurements and observations relative to the specified criteria.

5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

No MRMC comparative effectiveness study was done or is relevant to this type of device (Light Cure Composite). This is a material science and engineering performance evaluation, not a diagnostic imaging device requiring human reader input or comparison.

6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study

Not applicable. This device is a physical dental material, not a software algorithm.

7. Type of Ground Truth Used

The ground truth used for this study is based on established international standards (ISO 4049 and ISO 10993-1). These standards define the test methodologies and the acceptable performance limits for the specific physical and chemical properties of the dental composite material.

8. Sample Size for the Training Set

Not applicable. This is a hardware/material device, not an AI/ML algorithm that requires a "training set."

9. How the Ground Truth for the Training Set Was Established

Not applicable. As there is no training set for an algorithm, there's no ground truth to establish for it in this context.

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K Number

K001108

Device Name

PRIME-DENT VISIBLE LIGHT CURE COMPOSITE RESTORATIVE MATERIAL

Manufacturer

PRIME DENTAL MANUFACTURING, INC.