24 results · 27ms · Sources: EU EUDAMED, US FDA

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Vortek Single Loop Ureteral Stent

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003875·1000 micron Holmium Laser Fiber Cable, Reusable...

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383511735·"An absorbent paper points is an endodontic pap...

TTECH MODEL 200E + TENS DEVICE

FDA 510(k)
FDA Class 2 ·Neurology

AGILENT M2636A TELEMON MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

SOLITAIRE FR REVASCULARIZATION DEVICE

FDA Adverse Event
Injury ·COVIDIEN (IRVINE)·Product code NRY·August 25, 2015

GRANUFLO

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

NATURALYTE

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

ONYX

FDA Adverse Event
Injury ·COVIDIEN (IRVINE)·Product code MFE·February 18, 2015

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 27, 2014

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013

ENRHYTHM DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011

CONTOUR TRANSTAR STAPLER SET

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 2, 2018

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 24, 2014

INTERCEED (TC7) UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code MCN·October 20, 2020

ROD,FIXATION,INTRAMEDULLARY

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·May 8, 2018

ECHELON ENDOPATH STAPLER

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 25, 2019

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·November 18, 2019

ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 26, 2019