BEUDAMED
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    ABCO ULTRA SLIDE MICROSCOPE SLIDE

    FDA 510(k)
    FDA Class 1 ·Pathology

    Helix

    FDA UDI
    Nuvasive, Inc.·00887517134974·Helix R Plate, 32mm 2-Level

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777648·LUMBAMED BASIC DORSAL STAYS M SILVER II

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950018055·FORCEP WIRE LOOP #23 6" 15CM

    Elite Orthopaedics

    FDA UDI
    Elite Orthopaedics, Inc.·00816591013387·Post Op Telescoping Knee Brace

    RAZOR

    FDA UDI
    Ortho Arch Company Inc·D90980023212·RAZOR JARABAK PLIER

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197418782·Malleable Retractor Blade 51x152...

    ZOLL E SERIES 12SL, ANALYSIS OPTION

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOLDING FORCEPS

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·February 16, 2022

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·VERTIFLEX INC.·Product code NQO·April 3, 2020

    VEST MODEL

    FDA Adverse Event
    Injury ·Product code BYI·April 30, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·October 8, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 31, 2007

    Neodent GM X 6mm Engaging Titanium Base, REF: 9007162

    FDA Recall
    Open, Classified ·Preat Corp·Product code NHA·February 21, 2023

    Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay, Catalog Number 100018, Product is manufactured and distributed by Microgenics Corporation, located at Fremont, CA., part of Thermo Fisher Scientific The CEDIA Tobramycin II Assay is an in vitro diagnostic medical device intended for the quantitation of Tobramycin in human serum or plasma.

    FDA Recall
    Terminated ·Microgenics Corp·Product code LFW·October 16, 2013

    Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.

    FDA Recall
    Open, Classified ·Preat Corp·Product code NHA·April 2, 2025

    Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

    FDA Recall
    Open, Classified ·Preat Corp·Product code NHA·February 9, 2024

    NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662

    FDA Recall
    Open, Classified ·Preat Corp·Product code NHA·June 25, 2025

    Multigent Vancomycin Calibrators; Manufactured by Microgenics Corp, Fremont, CA. Distributed by: Abbott Diagnostics, Abbott Park, IL Product Usage: The Multigent Vancomycin calibrators are intended for use in the calibration of the multiagent vancomycin Vancomycin is a commonly used antibiotic to treat staphylococcus and other gram-positive bacterial infections.

    FDA Recall
    Terminated ·Microgenics Corp·Product code DLJ·June 8, 2011