17 results · 25ms · 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.

SATURN DENTAL IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

BIPOLAR FORCEPS

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

CYNOSURE PHOTOLIGHT PL

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

980 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·December 14, 2016

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC 12/14 Ø 28 SIZE L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 14, 2021

MPACT DM DOUBLE MOBILITY HC LINER Ø 50/28

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·July 30, 2019

LINER: MPACT DM DOUBLE MOBILITY HC LINER 22.2/DMC

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·December 7, 2020

DIMENSION® CLINICAL CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DIP·October 1, 2014

LMA LARYNGEAL MASK

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL ASIA PTE LTD·Product code CAE·May 23, 2013

DIAMOND II

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code DXY·June 16, 2011

LINER: MPACT DM DM CONVERTER TIN COATED D/DMB

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 27, 2024

STEM: M-VIZION PROXIMAL BODY Ø20MM L 90MM STD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 9, 2024

BD ULTRA FINE¿ INSULIN PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·June 1, 2018

CUP: MPACT ACETABULAR SHELL Ø56 MULTI-HOLE

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·March 1, 2022

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE M

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 13, 2022

MPACT DOUBLE MOBILITY SHELLS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·February 21, 2024

Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)

FDA Enforcement
Class II ·Ongoing·Medtronic Inc.·November 29, 2017