16 results · 26ms · Sources: EU EUDAMED, US FDA

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ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector

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

REKA E100

FDA 510(k)
FDA Class 2 ·Cardiovascular

T2 GREATER TROCHANTER NAIL

FDA 510(k)
FDA Class 2 ·Orthopedic

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 21, 2014

2520274-2013-03841

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·June 26, 2013

XCEL DILATING TIP TROCAR

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·August 4, 2011

DAMON Q

FDA Adverse Event
Injury ·ORMCO CORPORATION·Product code DYW·January 7, 2014

RHYTHMIA HDX

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·August 23, 2021

ULTRATHANE SUPRAPUBIC CATHETER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code KOB·August 23, 2022

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·March 17, 2022

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·March 17, 2022

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·March 17, 2022

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·March 17, 2022

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·August 23, 2021

COOK COPE-LOOP CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJE·July 21, 2021