35 results · 27ms · 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.

XTRA AUTOTRANSFUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

XTRA AUTOTRANSFUSION SYSTEM

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code CAC·August 2, 2021

Oticon

FDA UDI
Oticon A/S·05707131158338·VGPC, BTE 13 TC VIGO PRO CONNECT

IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

VENUS FREEZE SYSTEM

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

TAPERLC BMPC LAT 6.0X132 12/14

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

LUX 1440

FDA Adverse Event
Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

TAPERLOC PC 15.0 MM 12/14

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

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 1, 2013

HT70 PLUS VENTILATOR

FDA Adverse Event
Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·August 25, 2014

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

TAPERLOC COMPLETE MICROPLASTY FEMORAL

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

TPRLC 133 MP TYPE1 BM HO 10.0

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2019

TAPERLOC STEM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 19, 2017

TAPERLOC FEMORAL STEM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 22, 2016

TAPERLOC COMPLETE PRIMARY FEMORAL POROUS-BONEMASTER REDUCED DISTAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018