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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

4K CAMERA HEAD OLYMPUS CH-S400-XZ-EB, 4K AUTOCLAVABLE CAMERA HEAD OLYMPUS CH-S400-XZ-EA

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

n/a

FDA UDI
Ortho Development Corporation·00822409108169·Cement Only Broach Size 17

ECHELON TITANIUM HIP SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 4/10 MM R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 28, 2017

APEX KNEE

FDA Adverse Event
Injury ·OMNLIFE SCIENCE·Product code JWH·October 10, 2014

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2011

LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·June 17, 2013

FLEXOR URETERAL ACCESS SHEATH AND DILATORS

FDA Adverse Event
Malfunction ·COOK INC·Product code FED·January 3, 2020

FLEXOR URETERAL ACCESS SHEATH AND DILATORS

FDA Adverse Event
Malfunction ·COOK INC·Product code FED·January 2, 2020

FLEXOR URETERAL ACCESS SHEATH AND DILATORS

FDA Adverse Event
Malfunction ·COOK INC·Product code FED·January 7, 2020

FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 30, 2022

FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 30, 2022

BLACK SILICONE FILIFORM DOUBLE PIGTAIL URETERAL STENT

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·January 31, 2023

FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·January 2, 2020