38 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAP PLUS, EQUIVABONE, CAP/DBM
FDA 510(k)
FDA Class 2
·Orthopedic
TruForm
FDA UDI
Rmo, Inc.·00885797099815·MX 1-2 BI BD KT N/L UNIV 131
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450179536·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450638330·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450638309·
NITRILE PATIENT EXAMINATION GLOVE POWDER FREE, NON STERILE
FDA 510(k)
FDA Class 1
·General Hospital
LOGIQ 500
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 7, 2025
EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT-FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code ESW·March 25, 2015
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·April 26, 2013
CONSERVE(R) TOTAL HEAD W/BFH
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·May 6, 2011
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code LFL·July 24, 2008
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 2, 2017
UNKNOWN PATELLA
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·August 2, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM FEMORAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 2, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM ASSEMBLY
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·August 2, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 2, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM TIBIAL STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·August 2, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM FEMORAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·August 1, 2017
UNKNOWN ORTHOPAEDIC SALVAGE SYSTEM TIBIAL STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·August 1, 2017