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73 devices foundsorted by relevance

Manufacturer: U&I Corp. Clear all

  • CarePath System DCDUFD-001M

    I/O Urology Corporation,FDA registration: United States Class II
    None GUDID II

  • Umi (Franseen, Westcott, Greene, Menghini)Bio. Needle

    Universal Medical Instrument Corp.,United States(FDA 510(k) applicant) Not classified
    Active 510(k) 510(k) —

  • Us Aloka Ssd-256 Ultrasonic Scanner

    U. S. A. Imaging Corp.,United States(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Optima, Spinal System

    U&I Corp., America,United States(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Velofixtm Interbody Fusion System

    U&I Corp.,South Korea(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Latex Exam Gloves (Mfg: China Nat Chem Const Corp)

    Invent Ent. (U.S.A.) Corp.,FDA registration: United States Class I
    Active 510(k) 510(k) I

  • SECULOK™ ACP System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II
    2 variants

  • Chiropractic Massage Pillow

    Intl. Pacific Industrial Corp. (Usa), Inc.,FDA registration: United States Class I
    Active 510(k) 510(k) I

  • Benefix Interspinous Fixation System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II

  • Veloxtm Interbody Fusion System

    U&I Corp.,South Korea(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Amnio Centeses Kit W/Needle

    Universal Medical Instrument Corp.,United States(FDA 510(k) applicant) Class I
    Active 510(k) 510(k) I

  • Umi Steerable Torque Guide Wire

    Universal Medical Instrument Corp.,United States(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Nice Pack

    Universal Medical Instrument Corp.,United States(FDA 510(k) applicant) Class I
    Active 510(k) 510(k) I

  • Ssd-203 Ultrasonic Scanner

    U. S. A. Imaging Corp.,United States(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Maxima Anterior Cervical Plate System

    U&I Corp.,South Korea(FDA 510(k) applicant) Class II
    Active 510(k) 510(k) II

  • Aspiron Acp System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II

  • ANAX 5.5™ Spinal System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II

  • Perfix Iliac Screw System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II

  • Velofix TLIF Cage

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II
    2 variants

  • ANAX OCT Spinal System

    U&I Corporation,FDA registration: United States Class II
    Active 510(k) 510(k) II

Showing 1-20 of 73