BEUDAMED
    103 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW EXTRA STRENGTH CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW(R) EXTRA STRENGTH DAILY CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW EXTRA STRENGTH CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW EXTRA STRENGTH CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW(R) EXTRA STRENGTH DAILY CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·MIRAFLOW EXTRA STRENGTH CLEANER

    HydraLok

    FDA UDI
    Choice Spine, LP·10885862129376·

    Arx

    FDA UDI
    Life Spine, Inc.·00190837036317·ARX Thoracolumbar Screw Assembly; 8.5mm x 55mm

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209100132·KIT, TORK w' CHITOGAUZE - ODG

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008026944·PS, MIS-Tower, Cannulated Dual Lead 8.5X55mm. ...

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008027972·PS, MIS-Extend, Cannulated Cortical Cancellous ...

    A8 INTEGR8® Porous Pedicle Screw System

    FDA UDI
    ALLUMIN8, INC.·10850062071480·A8 INTEGR8 Cannulated Fenestrated Porous Pedicl...

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008029471·PS, MIS-Tower Reduction, Cannulated Dual Lead 8...

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008027125·PS, MIS-Tower, Cannulated Cortical Cancellous 8...

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008028474·PS, MIS-Extend, Cannulated Dual Lead 8.5X55mm. ...

    FOCUS

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00814008028979·PS, MIS-Tower Reduction, Cannulated Cortical Ca...

    PROFILE FEMORAL HIP

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    ARROW

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K