59 results · 22ms · Sources: EU EUDAMED, US FDA

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LOQTEQ LARGE FRAGMENT SET LOQTEQ CORTICAL SCREW 4.5, SMALL HEAD, T25, SELF TAPPING LOQTEQ CORTICAL SCREW 4.5, T25, SELF

FDA 510(k)
FDA Class 2 ·Orthopedic

COMPREHENSIVE SHOULDER SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304461123·

Bernafon

FDA UDI
Bernafon AG·05711584058350·SPEAKER UNIT, 4 L MEDIUM

Comprehensive® Shoulder System

FDA UDI
Biomet Orthopedics, LLC·00887868267925·

7450 RV2 MASK

FDA UDI
HANS RUDOLPH, INC.·00817136021447·7450 V2 PETITE W/HG & 2730 NRB

VIABAHN ENDOPROSTHESIS

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

COLLAGEN POWDER

FDA 510(k)
FDA Unclassified ·Unknown

COMPREHENSIVE REVERSE SHOULDER TITANIUM GLENOSPHERE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY WITH LOCKING RING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

COMPREHENSIVE REVERSE SHOULDER GLENOSHERE MINI BASEPLATE WITH TAPER ADAPTER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING ARCOMXL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 9, 2025

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 15, 2013

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS INC.·Product code CBK·September 17, 2014

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·June 3, 2011

LPV II VALVE, STANDARD SIZE, MEDIUM PRESSURE

FDA Adverse Event
Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·May 7, 2012

ARCOM XL 44-36 RTNV+3 HUMERAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 13, 2018

COMP RVRS SHLDR GLNSP STD 36MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PAO·August 29, 2017

VERSA-DIAL/COMP TI STD TAPER PR ADAPTOR

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code MBF·August 29, 2017

COMP RVRS SHDR GLEN BSPLT +HA

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PAO·August 29, 2017