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    Source-Ray, Inc.

    FDA registration
    Source-Ray, Inc.·4 products·🇺🇸 United States

    PXS-710D

    FDA UDI
    SOURCE-RAY, INC.·00868162000296·X-Ray System, General Purpose Podiatry

    SB-80-200R

    FDA UDI
    SOURCE-RAY, INC.·00868162000227·SourceBlock Assembly, 80kVp / 200uA

    XRS-125-7K-P

    FDA UDI
    SOURCE-RAY, INC.·00868162000210·X-Ray Source Assembly, 125kVp, 7ma / Pulsed

    UC-5000

    FDA UDI
    SOURCE-RAY, INC.·00867538000304·Mobile X-Ray System for General Purpose Radiogr...

    SR-130-C

    FDA UDI
    SOURCE-RAY, INC.·00868162000258·X-Ray Control, 100kVp / 30 mA

    XRS-140-15K-P

    FDA UDI
    SOURCE-RAY, INC.·00867538000311·X-ray Source Assembly, 140V, 15 mA- Pulsed

    SB-60-333

    FDA UDI
    SOURCE-RAY, INC.·00868162000203·SourceBlock Assembly, 60kVp / 333uA

    XRS-140-7.5K-P

    FDA UDI
    SOURCE-RAY, INC.·00867538000328·X-Ray Source Assembly, 140V, 7.5mA, Pulsed

    RC-115

    FDA UDI
    SOURCE-RAY, INC.·00868162000289·X-Ray Control, Remote

    SR-130-G

    FDA UDI
    SOURCE-RAY, INC.·00868162000241·X-Ray Generator / Tube Housing Assembly, 100kVp...

    SR-1260-G

    FDA UDI
    SOURCE-RAY, INC.·00868162000272·X-Ray Generator / Tube Housing Assembly, 120kVp...

    SR-1260-C

    FDA UDI
    SOURCE-RAY, INC.·00868162000265·X-Ray Control, 120 kVp / 60mA

    SR-115-CG

    FDA UDI
    SOURCE-RAY, INC.·00868162000234·X-Ray Control / Generator, 100 kVp/ 15mA

    COR20000302-000

    FDA Adverse Event
    Other ·Source-Ray, Inc.·Product code IZL·November 30, 2020

    7.0MM VARIABLE THREAD CANNULATED FASTENER

    FDA Adverse Event
    Malfunction ·OSTEOCENTRIC TECHNOLOGIES, INC.·Product code HWC·December 7, 2023

    NCB PLATE FOR FEMUR, LEFT, 5 HOLES

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·January 18, 2011

    NCB FULLY THREAD.CANCEL.SCREW

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·March 25, 2011

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·August 17, 2011

    DUROM US ACETABULAR COMPONENT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·November 8, 2010