16 results
·
29ms
·
Sources: EU EUDAMED, US FDA
M1350A FETAL MONITOR (INTRAPARTUM)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AppleCore™ Screws
FDA UDI
SPECIALTY APPLIANCES, LLC·D8199004800·
SOMATEX
FDA UDI
BIOPSYBELL SRL·08033860021771·
ACTIVE ELECTRODE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH
FDA 510(k)
FDA Class 2
·Anesthesiology
DS2ADV AUTO CPAP
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·May 27, 2024
DREAMSTATION 2 ADV AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 3, 2025
DS2ADV AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·October 8, 2024
DS2ADV AUTO CPAP
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·July 30, 2024
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 27, 2014
DEPUY ASR XL FEM IMP SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 7, 2013
KYPHOPLASTY
FDA Adverse Event
Injury
·MEDTRONIC SPINE LLC·Product code HRX·November 16, 2010
COMPREHENSIVE SHOULDER SYSTEM STANDARD TAPER ADAPTOR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017
HYBRID GLENOID POROUS TITANIUM GLENOID POST
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·April 28, 2017
COMPREHENSIVE SHOULDER SYSTEM MODULAR HEAD - VARIABLE OFFSET
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·November 21, 2023