59 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Vector Hammertoe Correction System
FDA 510(k)
FDA Class 2
·Orthopedic
NuVasive
FDA UDI
Nuvasive, Inc.·00195377046413·NTS Standard Tube, 18x50mm
Ion Coagulation Pen
FDA UDI
ION MEDICAL, INC.·B9122018502·18 Gauge Bipolar Coagulation Pen
CODMAN
FDA UDI
Cerenovus, Inc.·10886704002383·CODMAN AVM Micro Clip Applier No 1
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3
SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS
FDA 510(k)
FDA Class 2
·Dental
SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION
FDA 510(k)
FDA Class 2
·Anesthesiology
AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·April 2, 2019
AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·April 2, 2019
UNKNOWN SYMBOTEX MESH
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·May 2, 2019
UNKNOWN PARIETEX
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·May 2, 2019
VALIANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·July 17, 2018
VALIANT STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 17, 2018
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·August 11, 2011
ASCENSIA CONTOUR
FDA Adverse Event
Injury
·BAYER HEALTHCARE, LLC·Product code NBW·October 15, 2008
IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MTF·July 2, 2013
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·July 17, 2018
GMK SPHERE CEMENTLESS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MBH·May 25, 2026
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 21, 2024
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 5, 2025