17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES QUICK LOCK IMF SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Epredia
FDA UDI
NEW ERIE SCIENTIFIC LLC·00810041331915·
LEONE SPA
FDA UDI
LEONE SPA·08033707065722·INTRAORAL ELASTICS 4,5 oz 3/8" orange
ZAVATION
FDA UDI
Zavation LLC·00842166189669·Screw Driver, Angled
Soundwave Hearing
FDA UDI
Soundwave Hearing, LLC·00850016231222·RIGHT-SMALL/991004-SWH; replacement RIC for Son...
ZAVATION
FDA UDI
Zavation LLC·00842166118034·Awl - 2.0mm (0.078") diameter, 6mm tip length
RAPIDEC STAPH
FDA 510(k)
FDA Class 1
·Microbiology
Advocate Non-Contact Infrared Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
GUIDE PIN/SCREW
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613285145·
2520274-2013-01318
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 6, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·February 15, 2011
CAPSURE VDD 2
FDA Adverse Event
Injury
·MPRI·Product code DXY·August 8, 2014
SYNCHROMED UNKNOWN
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 12, 2011
HICKMAN/LEONARD/BROVIAC CENTRAL VENOUS CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·August 21, 2025
HICKMAN/LEONARD/BROVIAC CENTRAL VENOUS CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·August 21, 2025
ACHIEVE MAPPING CATHETER - 15 MM
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRF·August 30, 2019
Philips Zenition 50, Model Number: 718096
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024