77 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OLEEVA FOAM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002109·artVeneer life lower posteriors, XS, C2
BetaForce
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730021984·Beta3 Upper 18x18 10 archwires per pack
BetaForce™
FDA UDI
Ortho Organizers, Inc.·00190707124397·BETAFORCE Beta³ Upper 18x18 (10pk)
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112786·BARRON VACUUM PUNCH 8.25MM
Paragon 28
FDA UDI
Provision·B504OMP9910021090·
Baby Gorilla®/Gorilla® Plating System
FDA UDI
Paragon 28, Inc.·00889795019868·P28, Over drill, Ø2.1 x 90mm (Ø2.0), Solid, SS
INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PELVIS COIL
FDA 510(k)
FDA Class 2
·Radiology
HP M2376A DEVICE LINK SYSTEM, MODEL M2376A
FDA 510(k)
FDA Class 2
·Cardiovascular
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013
TOTALCARE BARIATRIC
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 4, 2011
ACCU-CHEK MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·February 20, 2008
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 1, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 10, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 6, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 5, 2011
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 14, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 14, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 7, 2010
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·July 7, 2011