33 results · 22ms · Sources: EU EUDAMED, 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