12 results
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25ms
·
Sources: EU EUDAMED, US FDA
T.C.S. TOTAL CONTACT SEAT
FDA 510(k)
FDA Class 1
·Physical Medicine
N/A
FDA UDI
Smith & Nephew, Inc.·00885556602430·MTO CANNULA - CARPAL TUNNEL
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193119618·HA PEEK EVOS Straight, ,13mmx9mmx 30mm , FLAT 1...
Master Series
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746094156·DB BRACKET MASTER SERIES MAND 1ST BICUSPID 018 ...
MILENIA (TM) DIGITOXIN
FDA 510(k)
FDA Class 2
·Clinical Toxicology
RADIOGRAPHIC FILM CASSETTE
FDA 510(k)
FDA Class 2
·Radiology
CROSSER RECANALIZATION CATHETER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·June 9, 2014
FEMORAL HEAD
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·January 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·November 22, 2010
25 G X 1 IN. ECLIPSE NEEDLE SMARTSLIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·November 21, 2019
smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·March 27, 2024
paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·October 2, 2024