15 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TORRENT IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768499·GENUMEDI PSS GREEN V
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017750·K-Wire, Double Ended, Trocar Point, Diameter 0....
BONASTENT® Tracheal/Bronchial
FDA UDI
Sewoon Medical Co., Ltd.·08806369468503·
AGILITY
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295035381·AGILITY LP TOTAL ANKLE SYSTEM TALAR SIZE 5 RIGH...
AGILITY
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295035411·AGILITY LP TOTAL ANKLE SYSTEM TALAR SIZE 5 LEFT...
CEM-OSTETIC PUTTY INJECTION KIT, MODEL PIK-XX, PIK-XX-YY
FDA 510(k)
FDA Class 2
·Orthopedic
FORA G90 PERFORM BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TAPERLOC COMPLETE PRIMARY FEMORAL 133 FP TYPE1 PPS HO 8.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·August 23, 2024
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code DTB·October 3, 2014
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 27, 2011
LD304 MATERNITY BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code HDD·May 31, 2013
BACT/ALERT MP - 419744
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code MDB·December 5, 2019
Radiomat Lightweight Cassettes
FDA Recall
Terminated
·AGFA Corp.·Product code IXA·January 26, 2005
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
FDA Enforcement
Class II
·Ongoing·Medtronic Inc.·November 29, 2017