BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Biolight ST kit

    Reg #: 3006697692 · FEI: 3006697692 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    20
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SYNCA MARKETING
    Registration Number
    3006697692
    FEI Number
    3006697692
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    337 Marion
    City
    Le Gardeur Quebec
    Country
    CA

    Owner / Operator

    Firm Name
    Synca Marketing
    Operator Number
    10034495
    Address
    337 Marion
    City
    Le Gardeur
    State
    Quebec
    Postal Code
    J5Z 4W8
    Country
    CA
    Correspondent
    Patrizia Manna

    US Agent

    Business Name
    Freeport Forwarding
    Contact Name
    Stephanie Brown
    Address
    1320 Route State 9
    City
    Champlain
    State
    NY
    ZIP
    12919
    Country
    US
    Email
    [email protected]
    Phone
    518 2988582

    Products

    Device Name Product Code
    Post, Root Canal ELR

    Proprietary Names

    Biolight ST kit Biolight Advanced Fiber Post Biolight Dual refill #0.5 Biolight Dual reamer #1 Biolight Dual kit Biolight Dual reamer #0.5 Biolight Dual refill #3 Biolight Dual reamer #2 Biolight ST reamer 1.50mm Biolight ST refill 10mm Biolight ST refill 1.20mm Biolight ST reamer 10mm Biolight ST reamer 1.35mm Biolight ST reamer 1.20mm Biolight ST refill 1.50mm Biolight ST refill 1.30mm Biolight Dual refill #1 Biolight Dual refill #2 Biolight Dual reamer #3 Biolight Drill Free

    Establishment Types

    Repack or Relabel Medical Device