16 results · 25ms · Sources: EU EUDAMED, US FDA

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Remington Medical Inc. Tuohy Epidural Needles

FDA 510(k)
FDA Class 2 ·Anesthesiology

Oticon

FDA UDI
Oticon A/S·05707131286635·RIA2 PRO, RITE 312 WL CBE

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690192497·Mod Tibia Starter Drill guide

IRIS Anterior Cervical Plate System

FDA UDI
Life Spine, Inc.·00190837060848·Cervical Screw Driver

IRIS Anterior Cervical Plate System

FDA UDI
Life Spine, Inc.·00190837060855·Cervical Screw Driver Shaft

Femoral Trial Size 3

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215073657·

ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603

FDA 510(k)
FDA Class 2 ·Cardiovascular

DIRECT BILIRUBIN LIQUICOLOR AND TOTAL BILIRUBIN LIQUICOLOR

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 20, 2025

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 12, 2026

2027971-2024-150266

FDA Adverse Event
Injury ·NOBEL BIOCARE USA, LLC·Product code DZE·November 29, 2024

OMNIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·May 29, 2013

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·July 6, 2011

EON MINI IPG, 16-CHANNEL RECHARGEABLE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 14, 2015

MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021

MULTI-PURPOSE ON-OFF FLUSHING VALVE W ASD, MEDIU

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES PR·Product code JXG·November 2, 2016