11 results
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18ms
·
Sources: EU EUDAMED, US FDA
STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407
FDA 510(k)
FDA Class 1
·Anesthesiology
MBT Pilot System - US IVD
FDA UDI
Bruker Daltonik GmbH·04251204326304·Visual support for manual sample preparation fo...
GC Initial™
FDA UDI
Gc America Inc.·J0228750581·GC Initial™ Zr-FS Dentin DB3, 20g
GC Initial™
FDA UDI
Gc America Inc.·15400556707422·GC Initial™ Zr-FS Dentin DB3, 20g
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668109571·DAHAN NUCLEUS PROLAPSING CANNULA
ABBOTT LIFECARE (R) 5000, PUMP SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID
FDA 510(k)
FDA Class 2
·Neurology
VICTORY XL DR
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·June 16, 2014
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 19, 2010
UNKNOWN DEPUY PINNACLE METAL LINER
FDA Adverse Event
Injury
·DEPUY IRELAND ¿ REG. # 9616671·Product code KWA·December 17, 2012
BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026