18 results · 57ms · Sources: EU EUDAMED, US FDA

MOBIS II spinal implant system (PEEK variant)

FDA registration
SIGNUS MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany

Synergy Health Allershausen GmbH

FDA registration
Synergy Health Allershausen GmbH·1 product·🇩🇪 Germany

Eurofins STERIPAC GMBH

FDA registration
Eurofins STERIPAC GMBH·1 product·🇩🇪 Germany

MOBIS II Spinal Implant System (Peek)

FDA registration
PROCON MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany

MOBIS II

FDA 510(k)
FDA Class 2 ·Orthopedic

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131372·TiBase AO WP 3.0G NE

MAHURKAR™ Chronic Carbothane™ Catheter Kit, Trays, and Sport Packs

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

ZIPPY SCOOTER

FDA registration
Guangdong Prestige Technology Co., Ltd.·1 product·🇨🇳 China

Cardinal Health Costa Rica, S.A.

FDA registration
Cardinal Health Costa Rica, S.A.·1 product·🇨🇷 Costa Rica

MAHURKAR Chronic Carbothane Catheter Kit, Trays, and Sport Packs

FDA registration
Covidien·1 product·🇲🇽 Mexico

Palindrome Chronic Catheter Kits and Sport Packs

FDA registration
MOZARC MEDICAL US LLC·1 product·🇺🇸 United States

MAHURKAR Chronic Carbothane Catheter Kit, Trays, and Sport Packs

FDA registration
Covidien LLC·1 product·🇺🇸 United States

Advanced Scar & Wound Hydrogel

FDA registration
Oculus Technologies of Mexico, S.A de C.V.·1 product·🇲🇽 Mexico

PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND DIGITAL WORKSTATION

FDA 510(k)
FDA Class 2 ·Radiology

DUOCOOL PAIN MANAGEMENT PROBE, MODEL OSP-17-180-20

FDA 510(k)
FDA Class 2 ·Neurology

Intervertebral Fusion Device With Bone Graft, Lumbar

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

Probe, Radiofrequency Lesion

FDA classification
FDA Class 2 ·Probe, Radiofrequency Lesion

System, Image Processing, Radiological

FDA classification
FDA Class 2 ·System, Image Processing, Radiological