70 results · 31ms · Sources: EU EUDAMED, 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