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510(k) Data Aggregation

    K Number
    K211307
    Device Name
    GalaSTITCH Absorbable Monofilament Suture
    Manufacturer
    Tepha, Inc.
    Date Cleared
    2021-05-27

    (28 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    GalaSTITCH™ Absorbable Monofilament Suture is indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery, or ophthalmic surgery.
    Device Description
    GalaSTITCH Absorbable Monofilament Suture (GalaSTITCH) is identical to the predicate TephaFLEX Absorbable Monofilament Suture (TephaFLEX) in regard to materials, design, and manufacturing processes. The product is being rebranded and will be commercialized by Tepha, Inc.'s wholly owned subsidiary, Galatea. GalaSTITCH is constructed of poly-4-hydroxybutyrate (P4HB) which is a biologically derived polymer that is extruded into monofilament fibers. The sterile P4HB suture is offered as undyed (clear) and dyed (violet) and meets all standards (except diameter) set by the United States Pharmacopeia (USP) for synthetic absorbable sutures. P4HB bioabsorbs through a process of hydrolysis and hydrolytic enzymatic digestion.
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    K Number
    K140533
    Device Name
    GALAFLEX MESH
    Manufacturer
    TEPHA, INC.
    Date Cleared
    2014-05-21

    (78 days)

    Product Code
    OOD
    Regulation Number
    878.3300
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    GalaFLEX mesh is indicated for use as a transitory scaffold for soft tissue support and to repair, elevate and reinforce deficiencies where weakness or voids exist that require the addition of material to obtain the desired surgical outcome. This includes reinforcement of soft tissue in plastic and reconstructive surgery, and general soft tissue reconstruction.
    Device Description
    GalaFLEX mesh is a sterile, knitted, resorbable mesh, constructed of non-dyed monofilament fibers made from poly-4-hydroxybutyrate (P4HB). It is provided in single sheets of varying widths, lengths and shapes, and may also be cut to the shape or size desired for a specific application.
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    K Number
    K132348
    Device Name
    TEPHAFLEX BRAIDED SUTURE
    Manufacturer
    TEPHA, INC.
    Date Cleared
    2013-09-05

    (38 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    TephaFLEX braided sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    TephaFLEX suture is a sterile, braided, surgical suture constructed of poly-4-hydroxybutyrate (P4HB). The suture consists of an inner core of multifilament fibers covered by a braided sheath made of multifilament fibers. The suture is provided dyed (D&C Violet No. 2) or un-dyed and is offered in a variety of cut lengths, with or without needles attached.
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    K Number
    K130422
    Device Name
    PHANTOM FIBER BIOFIBER SUTURE
    Manufacturer
    TORNIER, INC.
    Date Cleared
    2013-04-04

    (43 days)

    Product Code
    NWJ, ABS
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Phantom Fiber BioFiber Suture is indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    Tornier, Inc. Phantom Fiber BioFiber Suture is a n absorbable, braided, sterile, surgical USP size 2 suture composed of poly(4-hydrobutyrate) (P4HB) with cyanoacrylate adhesive tipped ends. Phantom Fiber BioFiber Suture is braided for optimal handling properties and is available either dyed (D&C Violet No. 2) or un-dyed (natural), with and without pre-attached needles.
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    K Number
    K122487
    Device Name
    BIOFIBER SYTURE
    Manufacturer
    TORNIER, INC.
    Date Cleared
    2012-09-17

    (33 days)

    Product Code
    NWJ, ABS
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    BioFiber Suture is indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    Tornier, Inc. BioFiber Suture is an absorbable, braided, sterile, surgical suture composed of poly(4-hydrobutyrate) (P4HB). BioFiber Suture is braided for optimal handling properties and is available either dyed (D&C Violet No. 2) or un-dyed (natural), with and without pre-attached needles.
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    K Number
    K100876
    Device Name
    AESCULAP MONOMAX ABSORBABLE SUTURE
    Manufacturer
    AESCULAP, INC.
    Date Cleared
    2010-07-14

    (106 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    MonoMax absorbable sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    The Aesculap® MonoMax Absorbable Sutures are sterile, monofilament, absorbable surgical sutures constructed of poly-4-hydroxybutyrate. The MonoMax sutures will be offered in sizes 2, 1, 0, 2-0, 3-0, 4-0, and 5-0. The sutures will be available in a variety of cut lengths with or without needles attached. The sutures will be available undyed, and dyed with the FDA approved colorant D&C Violet No.2 in accordance with Title 21 CFR, 74.3602.
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    K Number
    K082178
    Device Name
    TEPHAFLEX ABSORBABLE SUTURE
    Manufacturer
    TEPHA, INC.
    Date Cleared
    2008-10-30

    (90 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    TephaFLEX absorbable sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    TephaFLEX sutures are sterile, monofilament, absorbable surgical sutures constructed of poly-4-hydroxybutyrate. The TephaFLEX sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery, or ophthalmic surgery.
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    K Number
    K081099
    Device Name
    TEPHAFLEX ABSORBABLE SUTURE
    Manufacturer
    TEPHA, INC.
    Date Cleared
    2008-07-15

    (89 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    TephaFLEX absorbable sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    TephaFLEX suture is a sterile, monofilament, absorbable surgical suture constructed of poly-4-hydroxybutyrate. The TephaFLEX sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery, or ophthalmic surgery.
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    K Number
    K072470
    Device Name
    BIOELAST 5-0 SUTURE, MODEL 500100
    Manufacturer
    ENTRIGUE SURGICAL, INC.
    Date Cleared
    2007-11-16

    (73 days)

    Product Code
    NWJ
    Regulation Number
    878.4494
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    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    BioElast™ 5-0 absorbable sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular or neurological tissues, microsurgery or ophthalmic surgery.
    Device Description
    BioElast™ 5-0 Suture is a sterile, monofilament, absorbable surgical suture composed of poly-4-hydroxybutyrate. The BioElast™ 5-0 Sutures will be provided undyed at a 5-0 size.
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