23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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3M ESPE HAUR
FDA 510(k)
FDA Class 2
·Dental
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890107810·Zirlux Multi-Unit Abutment 1 mmH compatible wit...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450249802·
Medallion®
FDA UDI
Merit Medical Systems, Inc.·00884450096154·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237878·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237885·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237830·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237854·
CURRY MULTIMODAL NEUROIMAGING SOFTWARE
FDA 510(k)
FDA Class 2
·Neurology
DIRECT TIBC KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
M-VIZION FEMORAL REVISION SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·July 31, 2025
MEDICAL COMPRESSOR
FDA Adverse Event
Malfunction
·EKOM SPOL. S.R.O.·Product code BTI·April 5, 2011
4.3MM PERCUTANEOUS THREADED DRILL GUIDE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZX·March 19, 2013
UNKNOWN ZIMMER KNEE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·March 2, 2011
ATLAS II HF CRT-D
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 20, 2014
M-VIZION DISASSEMBLY ROD
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·April 20, 2022
CD HORIZON
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 16, 2016
BALL HEADS: MECTACER 01.29.209 BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE M
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·April 20, 2022
SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code MQP·October 30, 2017