AXERA Access System

FDA registration

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

ARSTASIS ONE LATCHWIRE ACCESS SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

NexxZr™ / W-98-35-UT-C400-ML

FDA UDI

SAGEMAX BIOCERAMICS, INC·00842271139610·

FlexStep

FDA UDI

Liftup A/S·05714420031432·FlexStep V2, 800, 5 step, indoor

PILOT DIODE LASER

FDA registration

CAO GROUP, INC.·2 products·🇺🇸 United States

Keratome, AC-Powered and / or Microkeratome Blades

FDA registration

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

PMT CORPORATION - STEREOTACTIC

FDA UDI

PMT CORPORATION·00650551098294·sEEG DEPTH ANCHOR BOLT DRIVER, FOR 2.4MM DRILL BIT

VOYAGER NC Dilatation Catheter

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

NICOLET WIRELESS EEG

FDA registration

Natus Neurology Incorporated·2 products·🇺🇸 United States

BENZODIAZEPINES

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

MILLENNIUM BLADES, MODEL MB101

FDA 510(k)

FDA Class 1 ·Ophthalmic

Introducer, Catheter

FDA classification

FDA Class 2 ·Introducer, Catheter

Keratome, Ac-Powered

FDA classification

FDA Class 1 ·Keratome, Ac-Powered

Enzyme Immunoassay, Benzodiazepine

FDA classification

FDA Class 2 ·Enzyme Immunoassay, Benzodiazepine