BEUDAMED
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    CENTRON CORPORATION

    FDA registration
    CENTRON CORPORATION·2 products·🇰🇷 South Korea

    MacoSeal SE160

    FDA UDI
    CENTRON CORPORATION·08809241443520·The MacoSeal SE160 is a specially designed tube...

    Rapid Seal Tube Sealer SE340

    FDA UDI
    CENTRON CORPORATION·08809241443124·The Rapid Seal SE340 is a multiple station benc...

    Rapid Seal Tube Sealer SE640

    FDA UDI
    CENTRON CORPORATION·08809241444527·The Rapid Seal Tube Sealer SE640 is a lightweig...

    Rapid Seal Tube Sealer SE530

    FDA UDI
    CENTRON CORPORATION·08809241441328·The Rapid Seal SE530 is a space saving bench-to...

    Rapid Seal Tube Sealer SE330

    FDA UDI
    CENTRON CORPORATION·08809241441229·The Rapid Seal Model SE330 is a standard bench-...

    Blood Collection Monitor CM350

    FDA UDI
    CENTRON CORPORATION·08809241446224·The Blood Collection Monitor CM350 is a blood c...

    Rapid Seal Tube Sealer SE540

    FDA UDI
    CENTRON CORPORATION·08809241443223·The Rapid Seal SE540 is a space saving bench-to...

    Blood Collection Mixer CM735A

    FDA UDI
    CENTRON CORPORATION·08809241446132·The Blood Collection Mixer CM735A is an automat...

    Rapid Seal Tube Sealer SE470

    FDA UDI
    CENTRON CORPORATION·08809241442233·The Rapid Seal SE470 is a compact and lightweig...

    Data Collection Mixer DCM3000 (BASIC)

    FDA UDI
    CENTRON CORPORATION·08809241446446·The Data Collection Mixer DCM3000 is an electro...

    CINTRON MEDICAL CORPORATION

    FDA registration
    CINTRON MEDICAL CORPORATION·1 product·🇺🇸 United States

    GI2000

    FDA UDI
    Cintron Medical Corporation·00860014201004·The gi2000 is an electrosurgical generator for ...

    CORRECT PLUS IMPRESSION MATERIAL

    FDA Adverse Event
    PENTRON / KERR CORPORATION·Product code ELW·July 27, 2018

    Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

    FDA Enforcement
    Class II ·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·June 12, 2019

    Kerr Maxcem Elite, self-etch/self-adhesive resin cement; Intro Kit Part No. 34417; DMC 0446 Rev 0. Used for cementation of all indirect restorations.

    FDA Enforcement
    Class II ·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·April 17, 2013

    NX3 Try-In Gel. The product is used as a tooth shade resin material.

    FDA Enforcement
    Class II ·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·September 25, 2013

    Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of this device is to be used for the cementation of indirect restorations including veneers, inlays, onlays, bridges, posts, and the cementation of crown restorations to implant abutments.

    FDA Enforcement
    Class II ·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·May 6, 2020

    37% Etching Gel-3ml syringe, part #N01H The intended use of these devices is to etch tooth dentin/enamel in order to prepare the tooth surface prior to the application of a bonding agent.

    FDA Recall
    Terminated ·Kerr/pentron Dba Kerr Corporation And Pentron Clinical·Product code EBF·March 31, 2011

    37% Etching Gel-1ml syringe 50 pk, part # T06B The intended use of these devices is to etch tooth dentin/enamel in order to prepare the tooth surface prior to the application of a bonding agent.

    FDA Recall
    Terminated ·Kerr/pentron Dba Kerr Corporation And Pentron Clinical·Product code EBF·March 31, 2011