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

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FLASH MINI OSTIAL SYSTEM - 3.0MM X 135CM, FLASH MINI OSTIAL SYSTEM - 3.5MM X 8MM X 135CM, FLASH MINI OSTIAL SYSTEM - 4.0

FDA 510(k)
FDA Class 2 ·Cardiovascular

PIVOX™ Oblique Lateral Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169605053·SPACER 2131450 OLIF25 27MM 6 DEG 14X50

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131450·MUA NC RP 2.5GH Str

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741314500·

Arthrex®

FDA UDI
ARTHREX, INC.·00888867107021·IBAL TKA TIB STEM,CM,14MM DX 50MM L

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674131450060·

VuMesh™

FDA UDI
Seaspine Orthopedics Corporation·10889981036690·End Cap (10mm Cage) 14mm, 5.0 Deg

CANTATA MICROCATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

QUANTA PLEX ENA PROFILE 6

FDA 510(k)
FDA Class 2 ·Immunology

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC 12/14 Ø 28 SIZE L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 14, 2021

MPACT DM DOUBLE MOBILITY HC LINER Ø 50/28

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·July 30, 2019

LINER: MPACT DM DOUBLE MOBILITY HC LINER 22.2/DMC

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·December 7, 2020

FINELINE II

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code DTB·October 1, 2014

PELVICOL 2CM X 7CM 1.0MM

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·May 10, 2013

ASKU

FDA Adverse Event
Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

LINER: MPACT DM DM CONVERTER TIN COATED D/DMB

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 27, 2024

CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·August 14, 2017

STEM: M-VIZION PROXIMAL BODY Ø20MM L 90MM STD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 9, 2024

IBALANCE TKA TIBIAL TRAY SIZE 6

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code JWH·March 8, 2017

IBALANCE TKA TIBIAL TRAY, SIZE 3

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code JWH·October 10, 2016