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AEROLET TOILET LIFT, MODEL AER-01

FDA 510(k)
FDA Class 2 ·Physical Medicine

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036023966·

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0310050·Probe, 1.5 inch Ball, Lenke, Curved, Black

InTess Lumbar Cage

FDA UDI
Kalitec Direct LLC·B07312K0310540·T-Handle, Primal, 1/4 inch Square, Cannulated

FloShield/Plus

FDA UDI
MINIMALLY INVASIVE DEVICES, INC.·00815128020553·The FloShield/Plus System is a single-use, disp...

ERA IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

TEXTURED POWDER-FREE LATEX EXAMINATION GLOVES CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GRAM

FDA 510(k)
FDA Class 1 ·General Hospital

MATRIX DETACHABLE COILS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·October 12, 2010

GDC DETACHABLE COIL

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code HCG·November 23, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code HCG·October 20, 2009

GDC-10 360 DEGREE COIL SR; GDC-10 360 DEGREE SOFT COIL SR; GDC-18 360 DEGREE COI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·May 18, 2010

GDC DETACHABLE COIL

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code HCG·June 17, 2009

MATRIX DETACHABLE COILS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·April 9, 2010

GUGLIELMI DETACHABLE COIL (GDC)

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·August 11, 2010

GDC-10 360 DEGREE COIL SR; GDC-10 360 DEGREE SOFT COIL SR; GDC-18 360 DEGREE COI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·July 20, 2010

GDC-10 360 DEGREE COIL SR; GDC-10 360 DEGREE SOFT COIL SR; GDC-18 360 DEGREE COI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·April 1, 2010

MATRIX DETACHABLE COILS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·May 17, 2010

LIGACLIP** ENDOSCOPIC CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·April 2, 2013

LANX SPINAL FIXATION SYSTEM

FDA Adverse Event
Injury ·LANX, LLC.·Product code NKB·March 22, 2011

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008