9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AST Model MA012 and MS019 Rehab Wheelchair
FDA 510(k)
FDA Class 1
·Physical Medicine
Oticon
FDA UDI
Oticon A/S·05707131330963·PRESCRIPTIVES 2017.1
NANOR AND EFFICAST/NANOR HYBRID THERMOPLASTIC MATERIALS
FDA 510(k)
FDA Class 2
·Radiology
CALCIUM HYDROXYLAPATITE VOCAL FOLD IMPLANT
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
E-Z CLEAN L-WIRE LAP 33CM
FDA Adverse Event
Malfunction
·MEGADYNE MEDICAL PRODUCTS, INC.·Product code GEI·August 13, 2018
TRULIANT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 14, 2025
ENDOSCOPIC MULTIFEED STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·October 17, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 27, 2011
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 6, 2013