45 results · 23ms · Sources: EU EUDAMED, US FDA

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HT III SA FIXTURE SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

andorate® 2-piece Cleaning Adapter + 4-piece Valve Kit

FDA UDI
GA Health Company Limited·04897106958023·

Surgical Kit

FDA UDI
BICON, LLC·00813110024077·Restorative Kit

Recon

FDA UDI
Revelation Medical Devices·G318101096100·1 Lb Mallet

Recon

FDA UDI
Revelation Medical Devices·G318101096200·Large Mallet

ABBOTT ACCLAIM ENCORE, MODEL 12237

FDA 510(k)
FDA Class 2 ·General Hospital

BURR HOLE COVER, MODEL XX

FDA 510(k)
FDA Class 2 ·Neurology

TAPERLC BMPC LAT 6.0X132 12/14

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

TAPERLOC PC 15.0 MM 12/14

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

FORTIFY VR

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

UNKNOWN HIP

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 19, 2014

PRECISION®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 24, 2011

ELECTRONIC GAS BLENDER

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025

TAPERLOC COMPLETE MICROPLASTY FEMORAL

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017

STOCKERT S3 GAS BLENDER

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014

LNCS DC-I

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code DQA·March 11, 2017

TPRLC 133 TYPE1 BM SO 11.0

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018

TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code KWA·May 26, 2017

TAPERLOC TYPE1 BM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018

TPRLC 133 FP TYPE1 BM HO 10.0

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018