BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    BOSWORTH LIQUID RESIN II

    K Number: K961200 · Decision May 17, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    166
    Registration Numbers
    166
    Same Product Code
    329
    Applicant Total
    45
    Review Days
    51

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    BOSWORTH LIQUID RESIN II
    K Number
    K961200
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3760
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Harry J. Bosworth Co.
    Date Received
    March 27, 1996
    Decision Date
    May 17, 1996
    Product Code
    EBI
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    EBI Resin, Denture, Relining, Repairing, Rebasing

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (EBI), ordered by most recent decision date.

    DB 4000 High Impact Denture Base

    FDA 510(k)
    FDA Class 2 ·Dental

    Denture Base

    FDA 510(k)
    FDA Class 2 ·Dental

    LuxCreo Flexible Partial Denture Resin

    FDA 510(k)
    FDA Class 2 ·Dental

    TERA HARZ Hard Denture (THD-C-500); TERA HARZ Hard Denture (THD-C-1000); TERA HARZ Hard Denture (THD-LP-500); TERA HARZ Hard Denture (THD-LP-1000); TERA HARZ Hard Denture (THD-P-500); TERA HARZ Hard Denture (THD-P-1000); TERA HARZ Hard Denture (THD-CP-500); TERA HARZ Hard Denture (THD-CP-1000)

    FDA 510(k)
    FDA Class 2 ·Dental

    UltraPrint-Dental Denture UV

    FDA 510(k)
    FDA Class 2 ·Dental

    Freeprint® denture flex

    FDA 510(k)
    FDA Class 2 ·Dental
    View all

    Other Clearances by Harry J. Bosworth Co.

    K Number Device Name
    K103585 BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP
    K100731 BOSWORTH AIR POLISHER
    K061611 BOSWORTH DENTIN RESIN
    K051224 BOSWORTH SEAL
    K043170 BOSWORTH BOND
    K040548 AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE
    K040547 AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE
    K033751 AEGIS PIT & FISSURE SEALANT WITH ACP
    K031439 ALGINATE IMPRESSION MATERIAL III (FAST & REGULAR)
    K031811 PIT & FISSURE SEALANT WITH FLUORIDE
    Search all 45 clearances from Harry J. Bosworth Co. →