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510(k) Data Aggregation

    K Number
    K232676

    Validate with FDA (Live)

    Date Cleared
    2024-01-23

    (144 days)

    Product Code
    Regulation Number
    872.6660
    Panel
    Dental
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    This product is indicated for use as a veneering material for fixed prosthesis in crowns, bridges.

    Device Description

    This product includes Porcelain Powder, Stain/Glaze and Blending liquid. The porcelain powder is composed of silica (SiOz), alumina (AlzOs), potassium oxide (K2O), sodium oxide (Na2O), boron trioxide (B2O3), calcium oxide (CaO), barium oxide (BaO), zirconia (ZrO2), zinc oxide (ZnO) , lithium oxide (Li₂O), tin oxide (SnO₂), magnesium oxide (MgO), Yttrium oxide (Y2O3) and terbium oxide (Tb2Os).. The blending liquid is composed of purified water, 1, 3-butanediol and diethanolamine. The Stain/Glaze is composed of the porcelain powder and the blending liquid in accordance with the mass ratio of 1:1.

    AI/ML Overview

    The provided text describes a 510(k) premarket notification for a "Dental Porcelain Powder" device and outlines its acceptance criteria and non-clinical testing results. It does not describe an AI/ML powered medical device, an imaging device, or a study involving human readers. Therefore, many of the requested categories are not applicable to this document.

    However, I can extract and present the information that is relevant to the acceptance criteria and non-clinical testing of this specific medical device.

    1. Table of Acceptance Criteria and Reported Device Performance

    ID#TestMethodAcceptance CriteriaReported Device PerformanceConclusion
    1.1Chemical composition of powderIngredient content analysisSilicon dioxide (SiO2): 57-67%Aluminum oxide (Al2O3): 10-20%Potassium oxide (K2O): 5-15%Sodium oxide (Na2O): 3-10%Boron trioxide (B2O3): 3-6%Calcium oxide (CaO): < 3%Barium oxide (BaO): < 3%Zirconium dioxide (ZrO2): < 3%Zinc oxide (ZnO): < 3%Other oxides: < 2%Met Product Technical RequirementsPass
    1.2UniformityVisual inspection after mixing/stirringPorcelain Powder: After mixing with blending liquid, no pigment separation.Stain/Glaze: After stirring evenly, no pigment separation.Met Product Technical RequirementsPass
    1.3SpecificationWeight measurementPorcelain Powder: (20g, 50g, 100g) ±0.5g/bottle.Stain/Glaze: (2g, 4g, 6g, 8g, 10g, 20g, 50g, 100g) ±0.5g/bottle.Met Product Technical RequirementsPass
    1.4No foreign bodyVisual inspectionPorcelain Powder, Stain/Glaze, Blending liquid should not be visible foreign bodies.Met Product Technical RequirementsPass
    1.5RadioactivityMeasurement of active concentrationPorcelain Powder and Stain/Glaze: active concentration of uranium-238 should be ≤1.0 Bq·g⁻¹.Met Product Technical RequirementsPass
    1.6Mixing and compacting propertiesEvaluation during mixing and dryingWhen porcelain powder is mixed with the blending liquid, it should not be caked or clumped. The blended paste, after being compacted layer by layer, should not crack or wrinkle during the drying process.Met Product Technical RequirementsPass
    1.7Flexural strengthMechanical testingPorcelain Powder, Stain/Glaze: should be ≥50 MPa.Met Product Technical RequirementsPass
    1.8Chemical solubilityChemical testingPorcelain Powder, Stain/Glaze: should be <100 ug·cm⁻².Met Product Technical RequirementsPass
    1.9Linear expansion coefficientThermal testingPorcelain Powder, Stain/Glaze: should be (10.3±0.5) ×10⁻⁶K⁻¹.Met Product Technical RequirementsPass
    1.10Glass transition temperaturesThermal testingPorcelain Powder, Stain/Glaze: should be (588±20)°C.Met Product Technical RequirementsPass
    1.11Bonding strength of veneer porcelainMechanical testingPorcelain Powder, Stain/Glaze: should be >20 MPa.Met Product Technical RequirementsPass
    1.12Blending liquid appearanceVisual inspectionThere should be no visible foreign body.Met Product Technical RequirementsPass
    1.13Blending liquid specificationVolume measurementIt should be ±1 mL.Met Product Technical RequirementsPass
    2.1CytotoxicityISO 10993-5:2009Non-cytotoxicNon-cytotoxicPass
    2.2Delayed hypersensitivityISO 10993-10:2010Non-Delayed hypersensitivityNon-Delayed hypersensitivityPass
    2.3Intradermal reactionISO 10993-10:2010Non-Intradermal reactionNon-Intradermal reactionPass
    2.4Acute systemic toxicityISO 10993-11:2017Non-Acute systemic toxicityNon-Acute systemic toxicityPass
    2.5Subchronic systemic toxicityISO 10993-11:2017Non-Acute systemic toxicityNon-Acute systemic toxicityPass
    2.6GenotoxicityISO 10993-3:2014Non-genotoxicityNon-genotoxicityPass

    Since this is not an AI/ML-powered or imaging device, the following categories are not applicable to the provided document. The device is a "Dental Porcelain Powder" and the testing described is non-clinical bench testing and biocompatibility testing.

    1. Sample size used for the test set and the data provenance (e.g., country of origin of the data, retrospective or prospective): Not applicable for this type of non-clinical, bench testing. The document does not specify sample sizes for individual tests but rather the acceptance criteria for material properties.
    2. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth for material properties is established by standardized testing methods, not expert consensus in this context.
    3. Adjudication method (e.g., 2+1, 3+1, none) for the test set: Not applicable.
    4. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance: Not applicable. No AI component.
    5. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done: Not applicable. No algorithm involved.
    6. The type of ground truth used (expert consensus, pathology, outcomes data, etc): Ground truth for the non-clinical tests is based on the specified physical, chemical, and biological properties as defined by relevant ISO standards and product technical requirements.
    7. The sample size for the training set: Not applicable. There is no training set as this is not an AI/ML device.
    8. How the ground truth for the training set was established: Not applicable.
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