94 results · 21ms · Sources: EU EUDAMED, US FDA

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DUAL SPIKE TRANSFER DEVICE

FDA 510(k)
FDA Class 2 ·General Hospital

Fast Threaded Guide Pin, 1.5mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665027488·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694002813·Micro Mesh, 74mm x 50mm

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613020194·Kurth Cilia Forceps, Angled Jaws, Overall Lengt...

RIVA Pedicle Screw System

FDA UDI
XENIX MEDICAL LLC·00840493418957·CONSTRAINED LORDOTIC ROD, 6.0mm x 150mm

RIVA Pedicle Screw System

FDA UDI
XENIX MEDICAL LLC·00840493418742·CONSTRAINED LORDOTIC ROD, 5.5mm x 150mm

EPOC READER & POWER SUPPLY

FDA Adverse Event
Malfunction ·EPOCAL INC.·Product code CGL·October 14, 2021

Coated Revision Stem

FDA UDI
SIGNAL MEDICAL CORPORATION·B046220811201500·20x150 Coated Revision Stem

Alliant Biotech

FDA UDI
MEDISURGE LLC·G611220811201500·Symmetric Total Knee Coated Revision Stem Size ...

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 18, 2021

CERAMICS2IN1

FDA 510(k)
FDA Class 2 ·Dental

CRC-15BT

FDA 510(k)
FDA Class 2 ·Radiology

2.0/1.0 4 hole long plate (titanium plate ).Lot 120150. Product labeling reads: (1. ) REF: 01-9205, Lot 999999, " 2.0MM" SYSTEM PLATE 4 HOLE PLATE, STRAIGHT, LONG. (2.) QTY 00001, CE 0086, *** NON-STERILE PRODUCT***, 1.0 MM TITANIUM, BIOMET MICROFIXATION, 1520 TRADEPORT DRIVE, JACKSONVILLE, FL 32218 USA, www.biometmicrofixation.com. (3.) #01-9205, LOT 999999, QTY 00001, 4 HOLE PLATE, STRAIGHT, LONG, 1.0 MM, CE 0086

FDA Recall
Terminated ·Biomet Microfixation, Inc.·Product code JEY·August 31, 2010

PERMACOL

FDA Adverse Event
Injury ·TISSUE SCIENCE LABORATORIES·Product code FTL·October 8, 2024

MINICAP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 20, 2013

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·September 25, 2014

BRYAN CERVICAL DISC SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MJO·June 10, 2011

SMART 120 150, SFA - 7X150MM

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code FGE·November 8, 2016

SMART 120 150, SFA - 7X150MM

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code FGE·October 3, 2016

SMART 120 150, SFA - 6X150MM

FDA Adverse Event
Injury ·CORDIS CORPORATION·Product code FGE·December 6, 2017