26 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CD Horizon Fenestrated Screw Set, CD Horizon Spinal System, Kyphon HV-R Bone Cement
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020
CD HORIZON SOLERA VOYAGER SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·May 27, 2024
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023288·270 Micron SU Thulio Performance 3m Fiber
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003097·270 micron Holmium Laser Fiber Cable, Single Us...
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003165·270 micron Holmium Laser Fiber Cable, Reusable,...
CoRoent
FDA UDI
Nuvasive, Inc.·00887517628367·CoRoent Ant TLIF Ti, 10x11x36mm 12°
AGXO
FDA UDI
Oticon A/S·05707131356994·G300 S, MINIRITE R LI-ION 2.4G C090 AGXO
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113967·HYDRO-DISSECT CANNULA 25GA ANGLED 7MM
AVANOS
FDA UDI
Avanos Medical, Inc.·00350770456997·CORFLO* Nasogastric/Nasointestinal Feeding Tube
LIPOSUCTION CANNULA
FDA UDI
SONTEC INSTRUMENTS, INC.·B0992013620·LIPOSUCTION CANNULA SPATULATED TIP
CORFLO ULTRA Lite NG
FDA UDI
CORPAK MEDSYSTEMS, INC.·10815149023073·Feeding tube, non weighted
LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KARL STORZ 3D VIDEO SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024
ADVANIX? BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 8, 2025
ADVANIX BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 30, 2024
COULTER LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·October 27, 2014
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 26, 2013