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