28 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Weck Auto Endo5 Hem-o-lok Ligating Clip Applier
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NA
FDA UDI
Gc America Inc.·10386040012393·PLUNGER FOR UNIVERSAL DISPENSER
NA
FDA UDI
Gc America Inc.·D6581520811·PLUNGER FOR UNIVERSAL DISPENSER
Staple Sizer - Orange
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215165253·
ENDOSCOPIC CLIP SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA
FDA 510(k)
FDA Class 2
·Cardiovascular
IDENTITY ADX XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·July 7, 2011
PELVICOL ACELLULAR COLLAGEN MATRIX
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTL·May 29, 2013
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
BD POSIFLUSH¿ NORMAL SALINE SYRINGES
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·March 31, 2022
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·July 19, 2019
ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W
FDA Enforcement
Class III
·Terminated·Ameditech Inc·December 30, 2015
PTA BALLOON CATHETER(OHICHO3)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 13, 2017
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 14, 2020