33 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BLADEWORKS MICROKERATOME BLADE, MODEL 7061
FDA 510(k)
FDA Class 1
·Ophthalmic
Channels
FDA UDI
HENRY SCHEIN, INC.·10304040038052·Channels K-Files 21mm, #40
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65820200791·Channels K-Files 21mm
Affiniti™ EH²
FDA UDI
TORNIER, INC.·00846832002191·
Midway Select
FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717100703·Earloop Masks Level 3 - White, Pkg/50
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036019105·
Premium Study Kit
FDA UDI
Cleveland Medical Devices Inc.·B14360200791·Single use, proact premium study kit.
NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MULTI-FUNCTION DEFIBRILLATION ELECTRODE
FDA 510(k)
FDA Class 3
·Cardiovascular
PROXIMATE RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.·Product code GAG·March 22, 2006
ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 3.5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·June 16, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·June 13, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·June 19, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006
45MM ARTICING LNR CUTR/BLUE RLD
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 21, 2005
ENDO LINEAR CUTTERS-ETS45MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·June 8, 2006
ENDOPATH ETS-FLEX45 ARTICULATING ENDOSCOPIC LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 15, 2006
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·December 30, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 1, 2014