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510(k) Data Aggregation

    K Number
    K253221

    Validate with FDA (Live)

    Device Name
    Liver fat ultrasound quantitative system, The FattaLab (FL-CC M1, FL-CC M1_Pro)
    Manufacturer
    Eieling Technology (Shenzhen) Limited
    Date Cleared
    2026-02-06

    (130 days)

    Product Code
    IYO
    Regulation Number
    892.1560
    Type
    Traditional
    Panel
    Radiology
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K251218

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    Device Name
    SafeBeat Rx App
    Manufacturer
    Safebeat Rx, Inc.
    Date Cleared
    2026-02-06

    (291 days)

    Product Code
    DQK
    Regulation Number
    870.1425
    Type
    Traditional
    Panel
    Cardiovascular
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K253959

    Validate with FDA (Live)

    Device Name
    Primevision 3D
    Manufacturer
    Dentsply Sirona
    Date Cleared
    2026-02-05

    (57 days)

    Product Code
    OAS
    Regulation Number
    892.1750
    Type
    Traditional
    Panel
    Radiology
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K260104

    Validate with FDA (Live)

    Device Name
    Signature™ ONE System
    Manufacturer
    Orthosoft Inc. (d/b/a) Zimmer CAS
    Date Cleared
    2026-02-04

    (22 days)

    Product Code
    QHE,HSD,KWS,KWT,MBF,PHX
    Regulation Number
    888.3660
    Type
    Special
    Panel
    Orthopedic
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K252438

    Validate with FDA (Live)

    Device Name
    Explant Express
    Manufacturer
    Applied Medical Technology, Inc.
    Date Cleared
    2026-02-03

    (186 days)

    Product Code
    QVS
    Regulation Number
    878.4675
    Type
    Traditional
    Panel
    General & Plastic Surgery
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K252676

    Validate with FDA (Live)

    Device Name
    The Circadia C300 System (C300)
    Manufacturer
    Circadia Health, Inc.
    Date Cleared
    2026-02-03

    (162 days)

    Product Code
    DRT
    Regulation Number
    870.2300
    Type
    Traditional
    Panel
    Cardiovascular
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K253640

    Validate with FDA (Live)

    Device Name
    T2 Alpha Femur Retrograde Nailing System; Pangea Femur Reconstruction System
    Manufacturer
    Stryker GmbH
    Date Cleared
    2026-02-03

    (76 days)

    Product Code
    HSB,HRS,HWC
    Regulation Number
    888.3020
    Type
    Traditional
    Panel
    Orthopedic
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K250644

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    Device Name
    MSS - Monobloc stem
    Manufacturer
    Medacta International S.A.
    Date Cleared
    2026-02-03

    (336 days)

    Product Code
    PHX
    Regulation Number
    888.3660
    Type
    Traditional
    Panel
    Orthopedic
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K251582

    Validate with FDA (Live)

    Device Name
    Redermax Antibacterial Wound Matrix
    Manufacturer
    Beijing Kreate Medical Co., Ltd.
    Date Cleared
    2026-02-02

    (255 days)

    Product Code
    FRO
    Regulation Number
    N/A
    Type
    Traditional
    Panel
    General & Plastic Surgery
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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    K Number
    K252011

    Validate with FDA (Live)

    Device Name
    CHIKAI Nexus petit
    Manufacturer
    Asahi Intecc Co., Ltd.
    Date Cleared
    2026-02-02

    (220 days)

    Product Code
    MOF
    Regulation Number
    870.1330
    Type
    Traditional
    Panel
    Neurology
    Age Range
    N/A
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
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