19 results · 31ms · Sources: EU EUDAMED, US FDA

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TRAP EASY

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

MITEK

FDA UDI
Medos International Sàrl·10886705029051·Sheath with 2 Rotating Stopcocks compatible wit...

MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

X-SERIES INTEGRAL RPP FEMORAL COMPONENTS

FDA 510(k)
FDA Class 2 ·Orthopedic

EASYTOUCH

FDA Adverse Event
Malfunction ·Product code FMF·December 20, 2024

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

BLUNT TIP SCREW, ÿ 4X38MM

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HSB·August 15, 2024

CLEARLINK

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2025

DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

FDA Enforcement
Class II ·Ongoing·DeRoyal Industries Inc·February 26, 2025

PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK

FDA Enforcement
Class II ·Terminated·MicroPort Orthopedics Inc.·June 8, 2022

BLUNT TIP SCREW, ÿ 4X34MM

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HSB·August 15, 2024

SPECIAL DEVICE UNITIZED PROGRA

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·July 15, 2020

ANN BLUNT TIP SCREW 4X46MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·September 23, 2025

4.0MM X 16MM VARIABLE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code KWQ·October 14, 2022

ANN BLUNT TIP SCREW 4X46MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·September 23, 2025

JGRKNT 1.0MM MINI 3-0 NDLS

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·May 27, 2025

4.0MM X 16MM VARIABLE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code KWQ·October 14, 2022