BEUDAMED
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    FIGUR8, INC.

    FDA registration
    FIGUR8, INC.·2 products·🇺🇸 United States

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·00862376000325·Single Straps Packaged Assembly

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·00862376000349·Sternotomy Closure Device (Shipper)

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·10862376000339·Shelf Box for Double Straps

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·10862376000322·Shelf Box for Single Straps

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·00862376000301·

    Figure 8 Sternotomy Closure Device

    FDA UDI
    FIGURE 8 SURGICAL, INC.·00862376000332·Double Straps Packaged Assembly

    COMPACT INTUITIV CONSOLE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·November 18, 2019

    21 GA LAMINAR PHACO TIP 30D SL REUSABLE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·November 18, 2019

    Bard Fluoro-4 Silicone Ureteral Stent, Bard¿ Fluoro-4", Silicone Ureteral Coil Stent; Bard¿ Silicone Uretera l Coil Stent with Figure Four, End, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.

    FDA Enforcement
    Class II ·Terminated·C.R. Bard, Inc.·November 23, 2016

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 17, 2026

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·September 30, 2011

    Bard Fluoro-4 Silicone Ureteral Stent, Bard Fluoro-4", Silicone Ureteral Coil Stent; Bard Silicone Uretera l Coil Stent with Figure Four, End, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.

    FDA Recall
    Terminated ·C.R. Bard, Inc.·Product code FAD·October 13, 2016

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 17, 2026

    VICRYL POLYGLACTIN 910 SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·October 8, 2025

    SEE H-10

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code HQL·December 16, 2015

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 29, 2024

    REBAR

    FDA Adverse Event
    Malfunction ·MEDTRONIC DOMINICANA·Product code KRA·March 21, 2025

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·October 29, 2022

    WHITESTAR SIGNATURE PRO CONSOLE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·November 13, 2019