30 results
·
20ms
·
Sources: EU EUDAMED, US FDA
THE IMPLEX HEDROCEL MODULAR ELLIPTICAL ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684KS0010391·
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741224317·Catheter Placement Kit
Reactive Air P.U. W/Tube Tridien US
FDA UDI
Tridien Medical·00841965103982·Reactive Air P.U. W/Tube Tridien US
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001039·artVeneer life upper anteriors, BS, A2
Two Light Blue VersaRing + Two VersaRods + Two VersaBlocks
FDA UDI
CLIKTECH LLC·00856200001039·Two Light Blue VersaRing + Two VersaRods + Two ...
Medstone
FDA UDI
Stille AB·07332339231507·TABLE, EXAMINATION, MEDICAL, POWERED
Enza
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030CB0010390·Intervertebral Locking Plate , 32mm x 38mm
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 18, 2025
INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MIDAS TOUCH BLUE NITRILE EXAMINATION GLOVES-POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024633186·
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024115200·
MultiPolar®
FDA UDI
Zimmer, Inc.·00889024115194·
PERCLOSE PROGLIDE 6F SUTURE CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·June 12, 2008
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 22, 2026
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·January 26, 2026
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
LEAD MODEL UNKNOWN
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 21, 2011
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Injury
·ELI LILLY AND CO.·Product code FMF·February 20, 2008