10,000 results · 34ms · 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.

OnePLUS Dental Implant

FDA UDI
OSSEOFUSE INTERNATIONAL, INC.·00810044842869·

REPLACE SELECT TAPERED PMC RP 4.3X11.5MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB GÖTEBORG·Product code DZE·September 3, 2025

O-ARM 1000 IMAGING SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OXO·February 8, 2019

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

GALILEO

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·October 11, 2006

GALILEO

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·May 8, 2006

UNK

FDA Adverse Event
Other ·UNK·Product code HDQ·February 24, 2000

O-SPOT

FDA Adverse Event
Malfunction ·BEEKLEY CORPORATION·Product code JAC·May 12, 2017

O-ARM O2 IMAGING SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OWB·August 28, 2018

SERIES TWENTY THOUSAND LEGACY

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECH CTR·Product code HQE·October 20, 2005

ALARIS® PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·November 29, 2018

CARDIOSAVE HYBRID, 3.1 EDITION

FDA Adverse Event
Malfunction ·DATASCOPE MAHWAH·Product code DSP·December 10, 2018

MEDTRONIC NAVIGATION

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·November 9, 2023

RSVR, PRDGM

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code LZG·May 31, 2006

6-0 POLYPROPYLENE SUTURE

FDA Adverse Event
Injury ·LUKENS MEDICAL CORPORATION·Product code GAW·January 10, 1994

GALILEO

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·May 8, 2006

2.3MM TAPERED ROUTER

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·September 6, 2022

HEMOCUE HB 201 DM SYSTEM

FDA Adverse Event
Injury ·HEMOCUE AB·Product code GKR·January 10, 2019

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·July 25, 2016

D2-40 (Lymphatic Marker); For In Vitro Diagnostic; Catalog number: PM266AA Product Usage: In Vitro Diagnostic Use.: a mouse monoclonal antibody that is intended for laboratory use in the qualitative identification of O-linked sialoglyprotein protein by immunohistochemistry (ICH) in formalin fixed paraffin embedded human tissues.

FDA Enforcement
Class III ·Terminated·Biocare Medical, LLC·June 3, 2015