21 results · 25ms · Sources: EU EUDAMED, US FDA

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STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Channels

FDA UDI
HENRY SCHEIN, INC.·10304040039134·Channels K-Files 25mm, #35

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·H65820200971·Channels K-Files 25mm

Megadyne

FDA UDI
MEGADYNE MEDICAL PRODUCTS, INC.·10614559104293·PCB Foot Control, For Mega Power Generator

Midway Select

FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717100994·Burs Finishing FG 7406, Pkg/5

POWDER-FREE NITRILE EXAMINATION GLOVES WITH ALOE VERA, GREEN (TESTED FOR USE WITH CHEMOTHERAPY DRUGS)

FDA 510(k)
FDA Class 1 ·General Hospital

GSI 2000 MIDDLE EAR ANALYZER

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code FRO·February 14, 2023

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code FRO·October 12, 2022

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 25, 2007

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 25, 2013

CENTRA BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·March 10, 2011

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code QSY·June 10, 2025

1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015

ASSEMBLY-ROTARY SCALE: 190-00126

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·January 2, 2019

ANSPACH INTEGRATION PACKAGING ASSEMBLY

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·March 19, 2019

UPS ASSY

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·March 19, 2019

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 16, 2019

Instructions For Use document of the GPS Trackers.

FDA Enforcement
Class II ·Terminated·Blue Ortho·November 4, 2020

Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

FDA Enforcement
Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012