16 results · 31ms · Sources: EU EUDAMED, US FDA

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FOOTPRINT ULTRA PK4.5MM AND 5.5MM SUTURE ANCHOR, SL

FDA 510(k)
FDA Class 2 ·Orthopedic

INTRA SKAN DC

FDA 510(k)
FDA Class 2 ·Dental

GAS SAMPLING LINES

FDA 510(k)
FDA Class 2 ·Anesthesiology

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

CHARGING SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013

3MM FLUTED BALL, 15CM

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·September 26, 2014

FLEXCATH STEERABLE SHEATH

FDA Adverse Event
Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·June 14, 2011

MEDTRONIC MINIMED 670G

FDA Adverse Event
Injury ·MEDTRONIC·Product code CGA·December 6, 2016

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

ARTIS Q ZEEGO

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 10, 2024

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