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

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Comprehensive Nano Stemless Shoulder

FDA 510(k)
FDA Class 2 ·Orthopedic

COMPREHENSIVE SHOULDER SYSTEM NANO HUMERAL COMP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·September 26, 2023

COMPR NANO HMRL PPS 34MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 10, 2024

COMPREHENSIVE SHOULDER SYSTEM NANO NUMERAL COMPONENT 30 MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·March 21, 2024

PERI-LOC PERIARTICULAR LOCKED PLATING SYSTEM HEXALOBULAR BONE SCREWS

FDA 510(k)
FDA Class 2 ·Orthopedic

LUCINA MODEL MELODI

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

AUTO LUBE SYSTEM

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEI·October 17, 2014

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 14, 2013

HUDSON INCENTIVE SPIROMETER LUNG VOLUME EXERC.

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BWF·July 8, 2011

PRUITT F3 CAROTID SHUNT

FDA Adverse Event
Malfunction ·LEMAITRE VASCULAR, INC.·Product code MJN·May 21, 2021

PRUITT F3 CAROTID SHUNT

FDA Adverse Event
Injury ·LEMAITRE VASCULAR, INC.·Product code MJN·May 21, 2021

PRUITT F3 CAROTID SHUNT

FDA Adverse Event
Malfunction ·LEMAITRE VASCULAR, INC.·Product code MJN·May 21, 2021

BD NANO¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 4, 2019

BD NANO¿ 2ND GEN PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 7, 2022

PRUITT F3 CAROTID SHUNT

FDA Adverse Event
Malfunction ·LEMAITRE VASCULAR, INC.·Product code MJN·April 23, 2021

BD ULTRA FINE PEN NEEDLES

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 11, 2020

PEN NDL 32G 4MM 5B XTW BULK US W/EXPIRY

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 13, 2020

BD ULTRA-FINE¿ MINI PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·February 5, 2019

BD¿ ULTRA-FINE PEN NEEDLES

FDA Adverse Event
Injury ·BECTON DICKINSON AND CO.·Product code FMI·January 24, 2019

RELION PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FMI·March 25, 2021