33 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Axeos
FDA 510(k)
FDA Class 2
·Radiology
Pantheon System
FDA UDI
ADLER ORTHO SPA·08050880238330·Pantheon Bridging Collar Ø 30 mm for Stem Ø 14 mm
Power Pin
FDA UDI
TP ORTHODONTICS INC·00192029028063·Stainless Steel
Taperloc® Complete
FDA UDI
Biomet Orthopedics, LLC·00887868565588·
Power Pin
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746056321·POWER PIN 50/PKG
LIPOSUCTION CANNULA
FDA UDI
SONTEC INSTRUMENTS, INC.·B0992011400·LIPOSUCTION CANNULA WITH THREE HOLES STRAIGHT
2.0MM SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036033736·
TAPERLOC COMPLETE RASP/PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304480872·
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820114000101·EXP ROTH 018/UR4&5 -7T 0A 2D
FOSSA EXPANDING DOUBLE PIGTAIL URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IDS5 IMAGE DISPLAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113905078·VICEROY Rod - 6.0 (D)6x(L)140mm
HammerTech
FDA UDI
FUSION ORTHOPEDICS, LLC·00852164007896·PEEK Implant Instrument Kit Medium
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·October 15, 2019
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 3, 2021
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 28, 2011
TRIAGE CARDIAC PROFILER KIT
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO INC·Product code MMI·April 5, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 29, 2011
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·July 2, 2013