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12 devices foundsorted by relevance

Manufacturer: Lca, Inc. Clear all

  • Hybrid Surgical Device Modification

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Closed End Fiberoptic Laser Delivery System

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cl-Ope Contact Laser System

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Laser Forceps Handpiece

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hybrid Surgical Device

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Snj Smoke Evacuation Suction Wand

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Alloy Scalpel Handpieces, Modification

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • The Hook-Curved Closed End/Elect Fiber Laser Deliv Sys

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Zoe Laser, Contact Nd:yag Laser System

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Molded Fiber Cap Delivery System

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Padless Electrosurgical Pencil

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Revised Labeling For Model Cl-0PE Nd:yag Laser

    Lca, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

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