16 results · 29ms · Sources: EU EUDAMED, US FDA

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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