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