iFuse Implant System (SI Joint Fusion System)

FDA registration

SI-BONE, INC.·1 product·🇺🇸 United States

MODIFICATION TO SI JOINT FUSION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Sacroiliac Joint Fixation

FDA classification

FDA Class 2 ·Sacroiliac Joint Fixation

NeuroTherm SMK Cannula

FDA registration

MIDWEST STERILIZATION CORP.·2 products·🇺🇸 United States

Intercept MICRO-PLATE EIA

FDA registration

ORASURE TECHNOLOGIES, INC.·1 product·🇺🇸 United States

SMK Radiofrequency Needle

FDA registration

St. Jude Medical, Cardiology Division, Inc.·2 products·🇺🇸 United States

SMK Radiofrequency Needle

FDA registration

St. Jude Medical, Atrial Fibrillation Division, Inc.·2 products·🇺🇸 United States

Intercept MICRO-PLATE EIA

FDA registration

ORASURE TECHNOLOGIES, INC.·1 product·🇺🇸 United States

SMK Radiofrequency Needle

FDA registration

Abbott Medical·2 products·🇺🇸 United States

Spinal needles and RF Cannula

FDA registration

Sterigenics Belgium Petit Rechain S.A.·2 products·🇧🇪 Belgium

Intercept MICRO-PLATE EIA

FDA registration

ORASURE TECHNOLOGIES, INC.·1 product·🇺🇸 United States

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450256466·

STC CANNABINOIDS INTERCEPT MICRO-PLATE EIA, MODEL 1118I

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

VAXCEL PORT, MODELS 45-336 AND 45-338

FDA 510(k)

FDA Class 2 ·General Hospital

Enzyme Immunoassay, Cannabinoids

FDA classification

FDA Class 2 ·Enzyme Immunoassay, Cannabinoids

Port & Catheter, Implanted, Subcutaneous, Intravascular

FDA classification

FDA Class 2 ·Port & Catheter, Implanted, Subcutaneous, Intravascular