BEUDAMED
    2,708 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·Artisan Myopia

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·ARTISAN-VERISYSE MYOPIA PHAKIC IOL

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·RINGJECT

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·OPHTEC-STABLEYES CAPSULAR TENSION RING

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·Capsular Tension Ring (CTR)

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·Capsular Tension Ring (CTR) and RingJect

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·Capsular Tension Ring (CTR)

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·RingJect

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·Artisan Myopia

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·ARTISAN/VERISYSE MYOPIA PHAKIC INTRAOCULAR LENS

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·ARTISAN (MODEL 206 AND 204) PHAKIC INTRAOCULAR LENS (PIOL) VERISYSE (VRSM5US AND VRSM6US) PHAKIC INTRAOCULAR LENS (PIOL)

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSULAR TENSION RING AND STABILEYES

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·ARTISAN MYOPIA PHAKIC IOL

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·RingJect and Capsular Tension Ring (CTR)

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·Artisan Myopia Intraocular Lens

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·ARTISAN/VERISYSE PHAKIC IOL

    Valve, Pulmonary

    FDA Pre-Market Approval
    FDA Class 3 ·Zephyr Endobronchial Valve (EBV) System

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL-KNEE(R) WITH CSTI(TM)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·COLLAGRAFT STRIP BONE GRAFT MATRIX