23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AEQUALIS REVERSED SHOULDER PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
MaXcess
FDA UDI
Nuvasive, Inc.·00887517177339·MaXcess Decomp Probe, Micro Ball
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317300065·
LEONE SPA
FDA UDI
LEONE SPA·08033707082330·BKT 42 F1000 SELF-LIGATING 22 T-6 A+2
OsteoMed
FDA UDI
OSTEOMED LLC·00845694025836·Genio Plate, 6mm, Rigid
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·November 8, 2001
OCO DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
Widex
FDA UDI
Widex A/S·05706069908176·WIDEX MOMENT MRB0 DEMO (Silver Grey ) 440, RIC 10
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·May 22, 2020
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·June 10, 2020
ARCHITECT C4000
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·October 26, 2021
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·December 13, 2021
PRECISION MONTAGE MRI
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 20, 2019
CONTOUR NEXT
FDA Adverse Event
Injury
·ASCENSIA DIABETES CARE US INC.·Product code NBW·January 10, 2017
PROGRASP FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·October 4, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·April 22, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·September 18, 2014
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code MMH·May 24, 2011
ARCHITECT C4000 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·June 12, 2017