Suturable DuraGen Dural Regenration Matrix

FDA registration

Integra LifeSciences Corporation·1 product·🇺🇸 United States

Suturable DuraGen Dural Regeneration Matrix

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

D187813

FDA registration

STERITECH, INC.·1 product·🇺🇸 United States

MAINLINE MEDICAL DENTAL SUPPLY

FDA registration

MAINLINE MEDICAL DENTAL SUPPLY·1 product·🇨🇦 Canada

Suturable DuraGen Dural Regenration Matrix

FDA registration

INTEGRA LIFESCIENCES CORPORATION·1 product·🇺🇸 United States

Suturable DuraGen Dural Regenration Matrix

FDA registration

Integra LifeSciences Corporation·1 product·🇺🇸 United States

Suturable DuraGen Dural Regenration Matrix

FDA registration

INTEGRA NEUROSCIENCES·1 product·🇺🇸 United States

DURAGEN II DURAL REGENERATION MATRIX

FDA 510(k)

FDA Class 2 ·Neurology

Dura Substitute

FDA classification

FDA Class 2 ·Dura Substitute

Fibrex

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Philips Medical Systems

FDA registration

GWW·1 product·🇩🇪 Germany

MODIFICATION TO:PHILIPS M3000A/M3046A COMPACT PORTABLE PATIENT MONITOR, MODELS PHILIPS M3000A/M3046A

FDA 510(k)

FDA Class 2 ·Cardiovascular

ZINC PHOSPHATE CEMENT

FDA 510(k)

FDA Class 2 ·Dental

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Cement, Dental

FDA classification

FDA Class 2 ·Cement, Dental