5,028 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RAYSCAN α
FDA UDI
Ray Co., Ltd·08800003000050·
OCL CONTOUR
FDA 510(k)
FDA Class 2
·Cardiovascular
EyeBOX
FDA UDI
Oculogica Inc.·00810051680003·Oculogica’s EyeBOX uses eye-tracking technology...
Phoenix Ultra Chain
FDA UDI
PHOENIX ORTHODONTICS INC·05060772895025·U CHAIN OPEN CLEAR SPOOL 15 FEET
OCL SPLINT
FDA Adverse Event
Injury
·OCL·Product code ILH·July 3, 1997
RAYSCAN α+
FDA UDI
Ray Co., Ltd·08800003001330·
OCL
FDA Adverse Event
Injury
·M-PACT WORLD WIDE MANAGEMENT·Product code FYH·November 17, 1999
OCL
FDA Adverse Event
Injury
·MEDICAL DEVICE MFG. & DISTRIBUTION·Product code FYH·February 5, 1998
RAYSCAN Studio
FDA UDI
Ray Co., Ltd·08800003004034·
RAYSCAN α
FDA UDI
Ray Co., Ltd·08800003000135·
OCL SPLINT
FDA Adverse Event
Injury
·M-PACT WORLDWIDE MGMT CORP·Product code FYH·May 17, 2001
UNKNOWN VAPR ELECTRODE
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code GEI·October 25, 2019
VISUAL-ICE CRYOABLATION SYSTEM
FDA Adverse Event
Malfunction
·BTG ROUND LAKE·Product code GEH·June 23, 2022
CARDIOSEAL OCL-040
FDA Adverse Event
Malfunction
·NMT NEUROSCIENCES IMPLANTS·Product code MGB·June 22, 2000
CARDIOSEAL OCL-023
FDA Adverse Event
Other
·NMT MEDICAL, INC.·Product code MLV·June 30, 2000
CARDIOSEAL OCL-028
FDA Adverse Event
Injury
·NMT MEDICAL, INC.·Product code MLV·October 27, 2000
OCL 22" LONG
FDA Adverse Event
Other
·M-PACT WORLDWIDE MANAGEMENT·Product code FYH·September 15, 1998
CARDIOSEAL OCL-017
FDA Adverse Event
Injury
·NMT MEDICAL INC.·Product code MLV·February 10, 2000
OCL SPLINT ROLL
FDA Adverse Event
Malfunction
·ORTHOPEDIC CASTING LAB, INC.·Product code LGF·September 19, 1994
OCL SPLINT ROLL
FDA Adverse Event
Injury
·M-PACT WORLDWIDE MGMT. CORP.·Product code LGH·August 21, 2001