wire, guide, catheter STANDARD 14 Guide Wire

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

ACS .010 HI-TORQUE INTER. AND STANDARD GUIDE WIRE

FDA 510(k)

FDA Class 2 ·Cardiovascular

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04049772814701·GENUMEDI SILVER SIZE VII

Fast Splint Matrix 1:1 compressible hybrid bulk refill (40)

FDA registration

SYNCA MARKETING·1 product·🇨🇦 Canada

Fiber Force products (repackaged product of Fast Splint)

FDA registration

BIO COMPOSANTS MEDICAUX (BCM)·1 product·🇫🇷 France

MACROPORE-PX PEDIATRIC SYSTEM

FDA registration

Medtronic Neurosurgery·1 product·🇺🇸 United States

Macropore PX Pediatric System

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

Rampart One Lumbar Interbody Fusion System

FDA UDI

SPINEOLOGY INC.·M7404902207·Rampart One Oblique Trial, 14mm, M, 8°

MULTIPLE AUTOANTIBODIES, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL

FDA registration

ZEUS SCIENTIFIC·1 product·🇺🇸 United States

RESTORELLE POLYPROPYLENE MESH

FDA 510(k)

FDA Class 3 ·Obstetrics/Gynecology

MACROPOREPX PEDIATRIC SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter

Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

FDA classification

FDA Class 3 ·Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

Plate, Bone

FDA classification

FDA Class 2 ·Plate, Bone