AIIFIM Implant System

FDA registration

COWELLMEDI CO., LTD.·1 product·🇰🇷 South Korea

ALLFIM IMPLANT SYSTEMS

FDA 510(k)

FDA Class 2 ·Dental

INTERLOK / HA COPELAND RESURFACING HEADS

FDA registration

BIOMET, INC.·2 products·🇺🇸 United States

CLASSIC CR SYSTEMS

FDA registration

Rayco (Shanghai) Medical Products Company Limited·1 product·🇨🇳 China

Kodak Directview CR System

FDA registration

CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·1 product·🇨🇦 Canada

iQ Body Fluids Module Key Disc Set (800-3016)

FDA registration

BECKMAN COULTER, INC.·1 product·🇺🇸 United States

NMT - Regional Block Adapter, 0.5m/1.5 ft.

FDA registration

RAUMEDIC Estonia AS·1 product·🇪🇪 Estonia

Elekta Neuromag®

FDA registration

MEGIN OY·3 products·🇫🇮 Finland

MODIFICATION TO HP M2376A DEVICE LINK SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

INTERLOK / HA COPELAND RESURFACING HEADS

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)