1,847 results
·
27ms
·
Sources: EU EUDAMED, US FDA
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly
FDA 510(k)
FDA Class 2
·Orthopedic
Darby Dental Supply, LLC
FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813525227·DERMASILK NITRILE GLOVE L
Autoimmune EIA
FDA UDI
BIO-RAD LABORATORIES, INC.·00847817018213·Autoimmune EIA Anti-Cardiolipin IgM Test Kit
JAWS Nitinol Staple System
FDA UDI
Paragon 28, Inc.·00889795049926·Straight Staple Assembly, 25 x 20mm
JAWS® Nitinol Staple System
FDA UDI
Paragon 28, Inc.·00889795124234·JAWs Great White Nitinol Staple System, 25 x 20...
Bindex BI-100
FDA 510(k)
FDA Class 2
·Radiology
HD-550 Video Endoscope System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - SMALL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·April 20, 2020
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LKK·December 4, 2008
MONOCRYL PLUS ANTIBACTERIAL SUTURES
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAN·September 16, 2011
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code DTB·July 29, 2013
ALARIS PCU MODULE
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·September 2, 2020
ALARIS PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·September 3, 2020
TBD
FDA Adverse Event
Injury
·SORIN GROUP ITALIA S.R.L.·Product code KRH·September 20, 2020
DREAMSTATION AUTO BIPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 31, 2022
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 2, 2020
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 2, 2020
FLANGE FIXTURE ST 4MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·February 24, 2020
ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 30, 2020
TACTICATH¿ QUARTZ CONTACT FORCE ABLATION CATHETER, 65MM
FDA Adverse Event
Malfunction
·VENUSA DE MEXICO S.A. DE C.V.·Product code OAE·September 2, 2022