BEUDAMED
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    P1 TECHNOLOGIES, INC.

    FDA registration
    P1 TECHNOLOGIES, INC.·4 products·🇺🇸 United States

    PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.

    FDA Recall
    Terminated ·Microport Orthopedics INC.·Product code LXH·April 30, 2014

    HOTLINE FLUID/BLOOD WARMER

    FDA Adverse Event
    LEVEL 1 TECHNOLOGIES, INC.·Product code LGZ·March 3, 1994

    LEVEL 1 NORMOTHERMIC IRRIGATING SYSTEM

    FDA Adverse Event
    Injury ·LEVEL 1 TECHNOLOGIES INC.·March 2, 1995

    LEVEL 1 HOT LINE

    FDA Adverse Event
    Malfunction ·LEVEL 1 TECHNOLOGIES, INC.·Product code BSB·September 27, 2002

    LEVEL 1 HOT LINE L-70

    FDA Adverse Event
    Malfunction ·LEVEL 1 TECHNOLOGIES, INC.·July 19, 1994

    HOT LINE FLUID WARMER

    FDA Adverse Event
    Malfunction ·LEVEL 1 TECHNOLOGIES, INC.·Product code LGZ·April 12, 1994

    HOTLINE FLUID WARMER

    FDA Adverse Event
    Malfunction ·LEVEL 1 TECHNOLOGIES, INC.·Product code LGZ·August 23, 1995

    WARMER DISPOSABLE SET

    FDA Adverse Event
    LEVEL 1 TECHNOLOGIES, INC.·Product code FPA·September 11, 1995

    FLUID WARMER

    FDA Adverse Event
    Malfunction ·LEVEL 1 TECHNOLOGIES, INC.·Product code LHC·March 19, 1996

    TOTAL HIP

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC.·Product code JDI·April 24, 2003

    TOTAL HIP

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC.·Product code JDI·April 24, 2003

    REVANESSE LIPS+ 1.2 ML

    FDA Adverse Event
    Injury ·PROLLENIUM MEDICAL TECHNOLOGIES·Product code LMH·November 2, 2022

    BATTERY,PAD-PAK-01

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·May 21, 2019

    ON-X AORTIC HEART VALVE WITH CONFORM-X SEWING RING AND EXTENDED HOLDER - 27/29MM

    FDA Adverse Event
    Injury ·ON-X LIFE TECHNOLOGIES, INC·Product code LWQ·September 16, 2016

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·August 27, 2025

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·March 17, 2025

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 17, 2026

    HEARTSINE GATEWAY 500P BUNDLE SALES BOM - UK ENGLISH

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·January 28, 2025

    INTELISWAB COVID-19 RAPID TEST

    FDA Adverse Event
    Malfunction ·ORASURE TECHNOLOGIES, INC·Product code QKP·January 12, 2023