18 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Epic 980
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741924300·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674192430060·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009775·2.4mm x 30mm Cannulated Lag Screw
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365117282·
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78819243000101·EXMRC ROTH 022/LR3 - 11T 7A 2M
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78819243000201·EXMRC MBT 022/LR3 - 6T 3A
TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET
FDA 510(k)
FDA Class 2
·Cardiovascular
1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML LUERL LOCK SAFETY SYRINGES
FDA 510(k)
FDA Class 2
·General Hospital
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070829·Cannulated 2.4 x 30mm Lag Screw Sterile Qty 5
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016
LIFEPAK(R) 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015
SOL-MILLENNIUM
FDA Adverse Event
Malfunction
·SOL-MILLENNIUM MEDICAL INC·Product code FMF·May 16, 2025
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014
MULTICARE PLATINUM
FDA Adverse Event
Injury
·HOLOGIC, INC.·Product code KNW·October 7, 2008
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 27, 2013
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·July 26, 2011
RHYTHMIA HDX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025