7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Benefix Interspinous Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
REMINGTON I-LIGHT HAIR REMOVAL SYSTEM
FDA Adverse Event
Injury
·SHASER INC·Product code ONF·May 21, 2021
MFP-051
FDA 510(k)
FDA Class 2
·Dental
SLEEPMINDER BREATHING FREQUENCY INDICATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 3, 2013
11.5FR X 13.5CM MAHURKAR KIT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOZ·October 6, 2014
PORTRAIT PSR3
FDA Adverse Event
Injury
·RHYTEC INC·Product code GEI·August 28, 2008