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

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EBI 5.5 HELICAL FLANGE SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

OMEGA-21 VERTEBRAL FIXATION SYSTEM

FDA Adverse Event
Malfunction ·BIOMET SPAIN, S.L.·Product code MNH·February 21, 2020

ROD, UNKNOWN SIZE

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

ILIAC SCREW, UNKNOWN SIZE

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

PEDICLE SCREW, UNKNOWN TYPE OR SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·August 30, 2021

UNKNOWN LUMBAR IMPLANT

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

CLOSURE TOP UNSPECIFIED

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

CLOSURE TOP UNSPECIFIED

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

CLOSURE TOP UNSPECIFIED

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code MNH·April 20, 2021

POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

POLARIS CURVED ROD, UNKNOWN

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

POLARIS CURVED ROD, UNKNOWN

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

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496061441·VENERE 70 OPEN TOE, SIZE XXL, SABBIA, GRADUATED...

SATURN BLOOD GLUCOSE MONITORING TEST STRIP

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

JAS CALCIUM (ARSENAZO) REAGENT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

EMAX 2 PLUS MOTOR

FDA Adverse Event
Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 10, 2013

AUTOCAT2 WAVE

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL, INC.·Product code DSP·March 16, 2011