5,028 results · 29ms · Sources: EU EUDAMED, US FDA

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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