10 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PALTOP DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
9300
FDA UDI
HANS RUDOLPH, INC.·00817136020150·9372 9327 LESS 9301 HD CNTRL
DIAMEDIX IS-ANTI-GLIADIN IGG TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
SIGNATURE PLANNER; SIGNATURE GUIDES
FDA 510(k)
FDA Class 2
·Orthopedic
BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 17, 2018
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD·Product code IOR·May 14, 2013
LINKED BEARING ASSEMBLY
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDC·May 18, 2011
ULTRACISION HARMONIC SCALPEL CURVED SHEARS, SCISSOR-GRIP HANDLE - 23 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GEI·August 12, 2008
BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 18, 2018
Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor
FDA Enforcement
Class II
·Terminated·Senseonics, Inc.·November 6, 2019