26 results · 34ms · Sources: EU EUDAMED, 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