156 results
·
28ms
·
Sources: EU EUDAMED, US FDA
COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690354·Titanium Straight Abutment Internal Hex. SP Ø5....
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193105048·HA PEEK EVOS Curved, , 15mmx10mmx 26mm , BICONV...
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690149·Advanced Dental Implant Ø5mm L13mm
Aligned Medical Solutions
FDA UDI
Aligned Medical Solutions·B09800700150·PERI PACK
SYNOX 53-15 BP
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO·Product code DXY·February 2, 2007
RETROX 45 JBP
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code DTB·February 2, 2007
PHILOS II SR
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code DTB·February 2, 2007
BARCOMED 2MP2
FDA 510(k)
FDA Class 2
·Radiology
INSTANT-VIEW METHADONE URINE CASSETTE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 29, 2024
4.5MM LCP PROXIMAL FEMUR PLATE 10 HOLES/283MM-LEFT
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·April 22, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 26, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE AND PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEMS
LOGIC CR TIB INSERT STD, SZ 3, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 3, 2024
ZENITH® TX2® TAA ENDOVASCULAR GRAFT PROXIMAL TAPERED COMPONENT
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code MIH·August 8, 2018
MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 21, 2022
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE V & PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEMS
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM (EECSS)