49 results · 24ms · Sources: EU EUDAMED, US FDA

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LONGEVITY IT HIGHLY CROSSLINKED POLYETHYLENE CONSTRAINED LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

HIGHLY CROSSLINKED POLYETHYLENE CONSTRAINED LINER

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KWZ·September 26, 2016

LID SPECULUM

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896088184·LID SPECULUM REVERSIBLE ADJUSTABLE ANGLED SHAF...

SureLOK Mini Posterior Cervical/Upper Thoracic System

FDA UDI
PRECISION SPINE, INC.·00840019907651·30mm Cervical Crosslink

Sterling Medical Products

FDA UDI
APOLLO MEDICAL PRODUCTS CORP.·00685404002982·HALSTEAD MOSQUITO FORCEP CURVED

Stradis Medical, LLC

FDA UDI
STRADIS MEDICAL, LLC·M752991017300·Mosquito Forceps

ACON PCP ONE-STEP PHENCYCLIDINE TEST STRIP, ACON PCP ONE-STEP PHENCYCLIDINE TEST DEVICE

FDA 510(k)
FDA Unclassified ·Unknown

GC FUJICEM

FDA 510(k)
FDA Class 2 ·Dental

OvertureTi

FDA UDI
Overture Orthopaedics·00810129551723·

OvertureTi

FDA UDI
Overture Orthopaedics·00810129550016·

BD LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 9, 2024

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·October 17, 2017

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·December 28, 2017

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·October 12, 2017

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·August 9, 2017

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·July 18, 2017

2800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 30, 2013

DBS LEAD

FDA Adverse Event
Malfunction ·MPROC, VILLALBA·Product code MHY·May 10, 2011

LIBERTE' MONORAIL CORONARY STENT DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code MAF·August 7, 2008