33 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
WIRELESS DR IMAGING OPTION-WDR1
FDA 510(k)
FDA Class 2
·Radiology
Synergy
FDA UDI
Rmo, Inc.·00885797101075·RMO(R) SYNERGY(R) BIOPROGRESSIVE H KIT .018 HK ...
Men's Liberty Acute
FDA UDI
ARGENTUM MEDICAL, LLC·00653599001943·Men's Liberty Acute Compatible with Suction
Arena-L®
FDA UDI
SPINEFRONTIER, INC.·00190361038757·Flat Trial Head, 35X26 Lordotic 12°, 15L
SURGICAL SYSTEM WITH CRYOGUIDE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ARSTASIS ACCESS SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
STARBURST SEMI-FLEX 3-5CM, 25CM LENGTH, FLEXIBLE
FDA Adverse Event
Injury
·ANGIODYNAMICS·Product code GEI·May 9, 2013
POWERLINK SYSTEM
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·Product code MIH·February 16, 2011
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026271·PLATEAU Interbody, Straight, Bulleted, 10mm 26m...
PLATEAU-TL
FDA UDI
Life Spine, Inc.·00190837028398·PLATEAU-TL Interbody, Convex, Bulleted, 10mm x ...
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·May 9, 2022
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785814·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785517·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785609·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785982·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246785906·
XMAX MOTOR
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code ERL·May 1, 2013
PLUM A+ DRIVER NEW
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 28, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 25, 2011
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615
FDA Recall
Terminated
·Product code GEI·December 19, 2014