1,549 results · 24ms · Sources: EU EUDAMED, US FDA

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HAPAD HEEL LIFTS - 3/4 LENGTH

FDA UDI
HAPAD INC·00082147001232·

LIAC HWL

FDA 510(k)
FDA Class 2 ·Radiology

ARCTIC SUN® 5000

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·December 23, 2022

ARCTIC SUN® 5000

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·May 17, 2021

ARCTIC SUN® 5000

FDA Adverse Event
Injury ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·July 16, 2021

ARCTICSUN 5000

FDA Adverse Event
Injury ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·February 12, 2020

ARCTIC SUN 5000

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·June 12, 2025

MODULAR HEAD COMPONENT 32MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 12, 2018

ARCOM 28MM RLOC LINER 10D/HWL 22

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 12, 2015

ARCOM 32MM RLOC LNR 10D/HWL 23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·December 27, 2017

ARCOM 28MM RLOC LNR 10D/HWL 22

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·November 26, 2014

ARCOM HEXLOC 28 10DEG W/HWL C

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 6, 2014

ARCOM 28MM RLOC LNR 10D/HWL 23

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·July 21, 2016

ARCOM HEXLOC 28 10DEG W/HWL A

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·February 12, 2015

ARCOM HEXLOC 28 10DEG W/HWL A

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 20, 2015

ARCOM 28MM RLOC LNR 10D/HWL 25

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 30, 2018

ARCOM 32MM RLOC LNR 10D/HWL 23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 7, 2021

ARCOM 28MM RINGLOC LINER 10D/HWL 21

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·May 11, 2015

TI LOW PROFILE SCREW 6.5X35MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 21, 2019

TI LOW PROFILE SCREW 6.5X35MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 21, 2019