15 results · 22ms · 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.

Boston ES (enflufocon A) Rigid Gas Permeable Contact Lens; Boston EO (enflufocon B) Rigid Gas Permeable Contact Lens; Boston XO (hexafocon A) Rigid Gas Permeable Contact Lens; Boston XO2 (hexafocon B) Rigid Gas Permeable Contact Lens

FDA 510(k)
FDA Class 2 ·Ophthalmic

MobileLink Acetabular Cup System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575187843·Surgical instrument handle, torque-limiting - M...

MobileLink Acetabular Cup System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575177127·Surgical instrument handle, torque-limiting - M...

PHENIX CERVICAL INTERBODY DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

STELLAR 150

FDA 510(k)
FDA Class 2 ·Anesthesiology

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

DEPUY ASR XL FEM IMP SIZE 53

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD.·Product code KXA·June 21, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

TRUEMETRIX

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·February 2, 2017

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·July 26, 2024

ROADRUNNER EXTRA-SUPPORT BARE MANDRIL WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQX·November 23, 2021

I-STAT EG7+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE INC.·Product code CHL·July 8, 2025

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 6, 2015

TRUE METRIX

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·March 22, 2022

ROADRUNNER EXTRA-SUPPORT BARE MANDRIL WIRE GUIDE

FDA Adverse Event
Injury ·COOK INC·Product code DQX·January 30, 2023