13 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Monoject
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517731005·CoRoent XL+, 10x18x45mm 15°
CoRoent
FDA UDI
Nuvasive, Inc.·00887517291981·CoRoent® XLFW, 10x22x45mm
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304477230·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694036184·Fusion K-wire/Drill Guide
Symmetry Rochester-Pean
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482056042·Symmetry® Forceps, Rochester-Pean, Straight, 18 in
CENTRO FAMILY OF MANUAL WHEELCHAIRS
FDA 510(k)
FDA Class 1
·Physical Medicine
REPROCESSED ELECTROPHYSIOLOGY CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
TRULIANT PS CEM FEM PS CEM RIGHT SZ 4.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 15, 2024
CAPSUREFIX
FDA Adverse Event
Malfunction
·MPRI·Product code NVN·October 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
UNICEL DXC 600I SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011
TRU CC FEMORAL SIZE 1 LEFT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 15, 2025