Metacross RX

FDA registration

Kaneka Corporation Osaka Plant·1 product·🇯🇵 Japan

Metacross RX PTA Balloon Dilitation Catheter

FDA 510(k)

FDA Class 2 ·Cardiovascular

Oticon

FDA UDI

Oticon A/S·05707131282293·H16V2 TI, BTE 13 WL 85 SGR

UNITY TOOL, INC.

FDA registration

UNITY TOOL, INC.·1 product·🇺🇸 United States

Trimethoprim/Sulfamethoxazole STREP (SXT) 0625/1.2-16/304 µg/mL

FDA registration

BECTON, DICKINSON & CO.·1 product·🇺🇸 United States

AVS Navigator PEEK Spacers

FDA registration

STRYKER SPINE·1 product·🇫🇷 France

AVS Navigator PEEK Spacers

FDA registration

STRYKER SPINE·1 product·🇺🇸 United States

BD FACSPresto System

FDA registration

Becton, Dickinson and Company, BD Biosciences·4 products·🇺🇸 United States

BD FACSPresto System

FDA registration

Becton Dickinson Caribe, LTD·4 products·🇺🇸 United States

BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-TRIMETHOPRIM-SULFAMETHOXAZOLE 0.0625/1.2-16/304 UG/ML

FDA 510(k)

FDA Class 2 ·Microbiology

AVA NAVIGATOR PEEK SPACERS, MODEL 48392XXX, 48393XXX

FDA 510(k)

FDA Class 2 ·Orthopedic

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA classification

FDA Class 2 ·System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar