16 results · 34ms · Sources: EU EUDAMED, US FDA

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STAYHEALTHY HEALTH KIOSK, STAYHEALTHY HEALTHCENTER KIOSK

FDA 510(k)
FDA Class 2 ·Cardiovascular

QUANTA SYSTEM DUOLITE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

STERI-SPOUTS; BAG-SPOUT, VIAL-SPOUT, TRANSFER MIXER; RAPIDFLOW, VIALFLOW, TRANSFLOW

FDA 510(k)
FDA Class 2 ·General Hospital

MUST LT 25MM LONG - PEDICLE SCREW Ø5X45 FENESTRATED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 7, 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

M2A 38MMX54MM CUP

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 22, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

PYXIS ANESTHESIA SYSTEM (PAS)

FDA Adverse Event
Malfunction ·CAREFUSION·Product code BRY·June 9, 2011

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