BIOSCREW XTRALOK

FDA registration

Linvatec Corporation d/b/a ConMed Linvatec·1 product·🇺🇸 United States

BioScrew XtraLok 8mm x 35mm

FDA registration

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

BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET

FDA 510(k)

FDA Class 2 ·Orthopedic

Revolution Peripheral Atherectomy System

FDA registration

REX MEDICAL LP·1 product·🇺🇸 United States

Trident Acetabular System

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

KEN-MAR MACHINE MFG CORP

FDA registration

KEN-MAR MACHINE MFG CORP·1 product·🇺🇸 United States

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450140505·

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450141014·

VOYAGER/VIPER WHEELCHAIR

FDA 510(k)

FDA Class 1 ·Physical Medicine

SILVERSPEED HYDROPHILIC GUIDEWIRE, MODELS 103-0601-300 AND 103-0602-300

FDA 510(k)

FDA Class 2 ·Cardiovascular

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone

Wheelchair, Mechanical

FDA classification

FDA Class 1 ·Wheelchair, Mechanical

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter