BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CAO GROUP, INC.

    Reg #: 1725006 · FEI: 3003258642 · Expires 2026
    View on FDA
    Products
    17
    Proprietary Names
    23
    Establishment Types
    6
    Classifications
    17

    Registration Details

    Registration Name
    CAO GROUP, INC.
    Registration Number
    1725006
    FEI Number
    3003258642
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    4628 WEST SKYHAWK DRIVE
    City
    W Jordan
    State
    UT
    ZIP
    84084
    Country
    US

    Regulatory Submissions

    510(k) Number
    K201475

    Owner / Operator

    Firm Name
    CAO Group, Inc.
    Operator Number
    9043755
    Address
    4628 West Skyhawk Drive
    City
    West Jordan
    State
    UT
    Postal Code
    84084
    Country
    US
    Correspondent
    Robert Larsen

    Products

    Device Name Product Code
    Massager, Vacuum, Radio Frequency Induced Heat PBX
    Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption OHV
    Laser, Dental, Soft Tissue NVK
    Heat Source For Bleaching Teeth EEG
    Powered Laser Surgical Instrument GEX
    Microscope, Surgical EPT
    Powder, Porcelain EIH
    Lamp, Infrared, Therapeutic Heating ILY
    Laser Activator For Polymerization QNF
    System, X-Ray, Extraoral Source, Digital MUH
    Activator, Ultraviolet, For Polymerization EBZ
    Non-Surgical Gown OEA
    Varnish, Cavity LBH
    Evacuator, Oral Cavity EHZ
    Agent, Tooth Bonding, Resin KLE
    Applicator, Resin KXR
    Clinical Electronic Thermometer SDV

    Proprietary Names

    Picasso Pro Diode Laser Hubble Digital Vision Upcera Lithium Disilicate Glass Ceramic Block Acuity Direct X-Ray Photon Detection SMARTLITE MAX PALMLIGHT 10, MODEL: 001-00030 ASCENT OLX ASCENT PX Hygea Diode Laser Aegis Protective Suit PILOT DIODE LASER LEAP Cavity Cleansing Solution Aegis Plume Evacuator FastFix BlissBond BlissEtch Visco Tip Liqua Tip FE Scrub Tip PRECISE LTM DENLASER 800 Precise SHP Diode Laser Aegis Infrared Thermometer

    Establishment Types

    Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Device in the United States for Export Only Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device for Another Party (Contract Manufacturer)