16 results · 22ms · Sources: EU EUDAMED, US FDA

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SIGMA High Performance (HP) Partial Knee System

FDA 510(k)
FDA Class 2 ·Orthopedic

DENOVO TEDDY GEL INFANT HEEL WARMER

FDA 510(k)
FDA Class 1 ·Physical Medicine

44MM E1 ACETABULAR LINER WITH 44MM BIOLOX DELTA OPTION CERAMIC HEAD OR 44MM M A MAGNUM

FDA 510(k)
FDA Class 2 ·Orthopedic

NEXTAR INFRARED CAMERA

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

LINER AND SHELL WITH PLASTIC BARRIER 48 MM I.D. 60 MM O.D.

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 3, 2023

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

STRATOS

FDA Adverse Event
Injury ·MEDXPERT GMBH·Product code HRS·September 11, 2014

RA CATH SET: 20 GA X 1-3/4"

FDA Adverse Event
Injury ·ARROW INTERNATIONAL, INC.·Product code DQX·October 4, 2007

ILIAC SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

POLARIS SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·December 3, 2020

POLARIS CURVED ROD, UNKNOWN

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·November 27, 2019

POLARIS TRANSLATION SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

POLARIS CURVED ROD, UNKNOWN

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·November 27, 2019