21 results
·
44ms
·
Sources: EU EUDAMED, US FDA
JOURNEY
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
JOURNEY II Uni Tibial Base and Insert
FDA registration
PERRYMAN COMPANY·1 product·🇺🇸 United States
JOURNEY
FDA registration
SMITH & NEPHEW, INC.·1 product·🇺🇸 United States
JOURNEY
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
JOURNEY II Uni Tibial Base and Insert
FDA 510(k)
FDA Class 2
·Orthopedic
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
SURGICAL INSTRUMENT MANUFACTURERS, LLC
FDA registration
SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States
Ergonomic Products Workstation
FDA registration
ERGONOMIC PRODUCTS, INC.·1 product·🇺🇸 United States
1.5 LACTOSORB SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036055189·
1.5 LACTOSORB SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036195298·
1.5 LactoSorb System
FDA UDI
BIOMET MICROFIXATION, INC·00888233025263·
Renew NCP-5 External Counterpulsation System
FDA registration
RENEW GROUP PRIVATE LIMITED·1 product·🇸🇬 Singapore
HeartLight Deflectable Sheath
FDA registration
STERILIZATION SERVICES OF VIRGINIA·2 products·🇺🇸 United States
QP-039P Afib Detection Program
FDA registration
NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States
QP-039P Afib Detection Program
FDA registration
NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan
Renew
FDA registration
S2 EQUIPMENT LLC·1 product·🇺🇸 United States
QP-039P Afib Detection Program
FDA registration
NIHON KOHDEN CORP.·1 product·🇯🇵 Japan
SIMTEC IM-MAXX 2 OPTION
FDA 510(k)
FDA Class 2
·Radiology
STAXX XDL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Spinal Vertebral Body Replacement Device
FDA classification
FDA Class 2
·Spinal Vertebral Body Replacement Device