Maxfire MarXmen

FDA registration

Sterigenics U.S., LLC·2 products·🇺🇸 United States

ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE

FDA registration

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

ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

MC2X¿ Three Stage Venous Cannula

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

QUADROSWITCH

FDA registration

KARL STORZ ENDOSCOPY-AMERICA, INC.·1 product·🇺🇸 United States

MC2X Three Stage Venous Cannula 29/29/29 FR with 3/8" Connector, Carmeda

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

QUADROSWITCH

FDA registration

Karl Storz Endoscopy-America, Inc.·1 product·🇺🇸 United States

Staple, Fixation, Bone

FDA classification

FDA Class 2 ·Staple, Fixation, Bone

Aneuroplastic

FDA registration

Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

Vertebroplastic Radiopaque Bone Cement

FDA registration

DEPUY CMW·1 product·🇬🇧 United Kingdom

KSEA QUADRO SWITCH

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

FDA 510(k)

FDA Class 2 ·Cardiovascular

Endoscopic Irrigation/Suction System

FDA classification

FDA Class 2 ·Endoscopic Irrigation/Suction System

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

FDA classification

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