32 results · 24ms · Sources: EU EUDAMED, US FDA

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ORTHOPEDIATRICS FRACTURE AND OSTEOTOMY BONE PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Depth gauge

FDA UDI
Jeil Medical Corporation·08809282818806·

MicroSelectron Digital

FDA UDI
Nucletron B.V.·08717213015692·microSelectron Transfer Tube for 4F Flexibles (14)

Summa Orthopaedics System Surgical Instrument

FDA UDI
Jeil Medical Corporation·08806390863247·

HARDYDISK BACITRACIN, 10MCG, MODEL Z927

FDA 510(k)
FDA Class 2 ·Microbiology

TAPERLOC COMPLETE

FDA 510(k)
FDA Class 3 ·Orthopedic

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

MAXCEM ELITE CLEAR

FDA Adverse Event
Malfunction ·KERR CORPORATION·Product code EMA·May 14, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 23, 2014

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·May 19, 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