33 results
·
18ms
·
Sources: EU EUDAMED, US FDA
CONTROL PLASMA N
FDA 510(k)
FDA Class 2
·Hematology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040093921·Maxima K-Files 21mm
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00126561·
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810012561·K-FILES 21MM #60
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496001256·MAGIC 50, SIZE S, MOKA, TIGHTS WITH A THREE-DIM...
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001256·artVeneer life lower anteriors, UBM, B3
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494462733·T-Handle
90mm x 90mm
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 26, 2026
OLYMPIC WARM-UP
FDA 510(k)
FDA Class 2
·Physical Medicine
CAP PORP, CAP TORP
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970157·
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
9616240-2006-00339
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00340
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00350
FDA Adverse Event
Malfunction
·Product code FII·June 23, 2006
9616240-2006-00345
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
LINEAR 3-6
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 19, 2020