Pruitt Inahara-Inahara Pruitt

FDA registration

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

PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Intravascular Occluding, Temporary

FDA classification

FDA Class 2 ·Catheter, Intravascular Occluding, Temporary

P.F.C. SIGMA

FDA UDI

DEPUY ORTHOPAEDICS, INC.·10603295233749·P.F.C. SIGMA FLUTED FEMORAL STEM 22mm x 175mm 5...

Alkaline Phosphatase (TRIS)

FDA registration

Fisher Diagnostics·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

PL Tubing Set (STERILE)

FDA registration

Engineered Medical Systems, LLC·1 product·🇺🇸 United States

Eye Shield

FDA UDI

KATENA PRODUCTS, INC.·00841668111147·FOX EYE SHIELD W/ GARTER PED PACK OF 50

NeuroPEN Endoscopic Shunt Placement Kit

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Acumed Bone Graft System

FDA registration

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

BinaxNow Strep A Test

FDA registration

ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·1 product·🇺🇸 United States

MODIFICATION TO: CARDIMA ABLATION SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

AccuLIF TL and PL Cage

FDA 510(k)

FDA Class 2 ·Orthopedic

Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

FDA classification

FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar