98 results · 21ms · Sources: EU EUDAMED, US FDA

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MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

K042172

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·September 2, 2022

DURACON PS LIPPED TIBIAL INSERT

FDA 510(k)
FDA Class 2 ·Orthopedic

POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·March 25, 2015

COVEREDGE 32

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 3, 2021

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

S-ROM M HEAD 36MM +0

FDA Adverse Event
Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·April 29, 2013

STANDARD MICRO INTRODUCER KIT

FDA Adverse Event
Malfunction ·ANGIODYNAMICS·Product code MSD·April 28, 2011

MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES·Product code LWR·July 24, 2008

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012