18 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Geistlich Derma-Gide
FDA 510(k)
FDA Unclassified
·Unknown
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWP·March 31, 2016
ORLUS MINI SCREW
FDA 510(k)
FDA Class 2
·Dental
PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
MUSTMINI OCCIPITAL SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025
CADD LEGACY PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·April 11, 2022
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 8, 2022
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 23, 2022
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 22, 2022
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·October 17, 2014
ENDOPATH** XCEL* TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·July 28, 2011
PROPAQ MD DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code LDD·June 11, 2013
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 22, 2022
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 8, 2022
CADD LEGACY PLUS PUMPS
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·October 29, 2022
CADD LEGACY PLUS PUMPS
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·October 24, 2022
MUSTMINI OCCIPITAL SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025
MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024