70 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT IN ZIRCONIA, ATLANTIS GEMEINI + ABUTMENT IN ZIRCONIA
FDA 510(k)
FDA Class 2
·Dental
Armada
FDA UDI
Nuvasive, Inc.·00887517208637·ARM15T Rod, 70mm Conventional Pre-Bent
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809849431·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE LARGE FU...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197532839·Vascular Metzenbaum Scissors
Ø5mm, ...
BIOLOK SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
ORALLITE COMPREHENSIVE EXAM TRAY
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·October 31, 2025
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 19, 2026
HARMONIC FOCUS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code LFL·March 29, 2013
TERUMO CDI 540 CALIBRATOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·March 1, 2011
MIDDLE SCREW EXTENDER SLEEVE
FDA Adverse Event
Malfunction
·ABBOTT SPINE·Product code LXH·May 21, 2008
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 1, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 14, 2026
SYRINGE 1ML LL W/NDL ECLIPSE 27X1/2 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·August 5, 2019
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 9, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 22, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·April 3, 2026
MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·November 4, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 22, 2025