11 results
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26ms
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Sources: EU EUDAMED, US FDA
DUODERM(R) HYDROACTIVE(R) PASTE
FDA 510(k)
FDA Unclassified
·Unknown
LinkSymphoKnee - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575314416·Orthopaedic prosthesis implantation instrument,...
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011881302220·dentaform® Snap, tooth 36, size 2/Roth 22
LinkSymphoKnee - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575314393·Orthopaedic prosthesis implantation instrument,...
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011881302180·dentaform® Snap Band, tooth 36, size 2/Roth 18
RESCUE EXTERNAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Bodycad Unicompartmental Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
GYNECARE TVT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 18, 2014
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 18, 2010
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·December 20, 2012
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026