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

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REACH ACCESS TELEMEDICINE DOSE CALCULATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814206·GENUMEDI PT SILVER L III

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550124·GENUMEDI PT KNEE SUP SILVER L EW III

VIZION DR

FDA 510(k)
FDA Class 2 ·Radiology

6-8MM X 30 MM INTRAFIX PEEK TAPERED SCREW 7-9MM X 30MM INTRAFIX PEEK TAPERED SCREW 8-10MM X 30 MM INTRAFIX PEEK TAPERED

FDA 510(k)
FDA Class 2 ·Orthopedic

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

LAMITRODE TRIPOLE 16

FDA Adverse Event
Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013

LIBERTY CYCLER SET SINGLE CONN/EXT

FDA Adverse Event
Malfunction ·REYNOSA MANUFACTURING·Product code FKX·May 26, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

POLARIS SCREW, UNKNOWN SIZE

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

PEDICLE SCREW UNSPECIFIED

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

PEDICLE SCREW UNSPECIFIED

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

SOLETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 19, 2014

ESOPHYX Z

FDA Adverse Event
Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

PEDICLE SCREW UNKNOWN TYPE/SIZE

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

CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

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

POLARIS TRANSLATION SCREW, UNKNOWN SIZE

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