Kogent Bipolar Forceps

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

Focused Irrigating Bipolar Forceps

FDA registration

KATALYST SURGICAL, LLC·1 product·🇺🇸 United States

KOGENT BIPOLAR FORCEPS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ReForm Pedicle Screw System

FDA registration

NUTECH SPINE, INC.·2 products·🇺🇸 United States

REFORM PSS SYSTEM

FDA registration

Precision Spine, Inc.·2 products·🇺🇸 United States

Validate PSA product code 406bc

FDA registration

LGC Clinical Diagnostics, Inc.·1 product·🇺🇸 United States

CULVER TOOL & ENGINEERING

FDA registration

CULVER TOOL & ENGINEERING·2 products·🇺🇸 United States

Teleflex Medical LLC

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

UniTip Catheter

FDA UDI

Unisensor AG·07640172973790·

UniTip Catheter

FDA UDI

Unisensor AG·07640172973875·

REFORM PEDICLE SCREW SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

CIV-OB (PLUS)

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Electrosurgical, Cutting & Coagulation & Accessories

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories

System, Monitoring, Perinatal

FDA classification

FDA Class 2 ·System, Monitoring, Perinatal

Orthosis, Spinal Pedicle Fixation

FDA classification

FDA Class 2 ·Orthosis, Spinal Pedicle Fixation