38 results · 26ms · Sources: EU EUDAMED, 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