36 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DR-HO'S Electro Therapy Conductive Gel
FDA 510(k)
FDA Class 2
·Neurology
Tether
FDA UDI
Seaspine Orthopedics Corporation·10889981101749·Var. Angle Screw Driver
OsteoMed
FDA UDI
OSTEOMED LLC·00845694036337·Hohmann Retractor, 6" w/ 15mm Blade
PAR SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896054943·PAR SCISSORS CURVED BLADES POWER CUT GOLD
TMC SpeedTMT
FDA UDI
Treace Medical Concepts, Inc.·00810111225175·Inserter Cap
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869611718·MOSS VRS head alignment aid
Histofluor® Rodent LKS Fluorescent Antibody Test System
FDA UDI
IMMUNO CONCEPTS INC·M7491200402101·Mouse LKS 4 Well Tiissue Slides - 10 Slides
SCREENERS PHENCYCLIDINE (PCP) TEST, DRUGSCREEN DIP PHENCYCLIDINE (PCP) TEST
FDA 510(k)
FDA Unclassified
·Unknown
SITE-RITE VISION ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·March 29, 2023
BOSTON SIMPLICITY
FDA Adverse Event
Injury
·POLYMER TECHNOLOGY USA·Product code LPN·October 28, 2002
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 28, 2025
ANEURX XPEDIENT ILIAC SG
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·October 20, 2017
COULTER ACT DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·February 10, 2016
RESTORATION ADM X3 INS 28/50
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·October 24, 2014
XPERT SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code FGE·August 11, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JUMAO MEDICAL EQUIPMENT·Product code IOR·July 1, 2013
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 19, 2022
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Death
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 19, 2022
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·September 17, 2019