23 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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JAMSHIDI BIOPSY NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Diamond D
FDA UDI
Keystone Industries·H66810130701·Denture Acrylic HC Light 25 lb P&L
NuVasive
FDA UDI
Nuvasive, Inc.·00887517071279·Universal Articulating Arm, Micro
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453704·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453674·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453681·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453698·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453667·
CorticaLINK
FDA UDI
LINKSPINE, INC.·00817329020479·5.0mm Titanium Rod: 70mm Curved
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453643·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033453650·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0130001·PLATE BENDER, UNIVERSAL
SYNCHRON VANCOMYCIN REAGENT
FDA Adverse Event
BECKMAN COULTER INC.·Product code LEH·June 10, 2011
ETHIBOND EXCEL VALVE LOOP SUTURE
FDA 510(k)
FDA Class 2
·Cardiovascular
ULTRAPAK NEHA
FDA 510(k)
FDA Unclassified
·Unknown
MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·March 15, 2013
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
TRANSEND 300 FLOPPY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·February 27, 2008
ARROW OnControl Bone Lesion Biopsy System Tray, Sterile, Rx only, The Arrow OnControl Bone Lesion Biopsy System is intended for bone biopsy of the vertebral body and bone lesions.
FDA Enforcement
Class II
·Terminated·Teleflex Medical·December 7, 2016
Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is indicated for use in pediatric craniotomy flap fixation.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·May 16, 2018