BEUDAMED
    FDA Registration Active 🇺🇸 United States

    JKR LABORATORIES, INC.

    Reg #: 1929340 · FEI: 1929340 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    20
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    JKR LABORATORIES, INC.
    Registration Number
    1929340
    FEI Number
    1929340
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    10701 W Kellogg St
    City
    WICHITA
    State
    KS
    ZIP
    67209
    Country
    US

    Owner / Operator

    Firm Name
    JKR LABORATORIES, INC.
    Operator Number
    1929340
    Address
    10701 WEST KELLOGG
    City
    Wichita
    State
    KS
    Postal Code
    67209
    Country
    US
    Correspondent
    Lynette M Sundeen

    Products

    Device Name Product Code
    Syringe, Ent KCP
    Hearing Aid, Air-Conduction, Prescription ESD

    Proprietary Names

    #102 XL Impression Syringe Handy Handle Red Handy Handle Blue #102S XL Spare Cylinder, Transparent #97A Gold Velvet II 40 unit #98 XL-300 Impression Kit 660 g #108 Gold Velvet II Impression Singles 8 g #107A Blue Ultra Cartridge 8 x 50 ml #107C Pink Ultra Cartridge 8 x 50 ml #108 Gold Velvet II Impression Single 2x8 g #100 XL-100 Impression Kit 660 g #103D Aqua Plus Single Red 2x8 g #103 Aqua Plus Kit #103E Aqua Plus Single Blue 2x8 g #97 Gold Velvet II 10 unit #97B Gold Velvet II 80 unit #99 XL-200 Impression Kit 660 g Labeled under JKR Laboratories, Inc: #98A XL Catalyst Paste 25 g #98A XL-300 Accelerator 25 g

    Establishment Types

    Repack or Relabel Medical Device