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    NSE PRODUCTS, INC.

    FDA registration
    NSE PRODUCTS, INC.·3 products·🇺🇸 United States

    Nu Skin RenuSpa iO Package

    FDA UDI
    NSE PRODUCTS, INC.·00850021097561·

    Nu Skin RenuSpa iO

    FDA UDI
    NSE PRODUCTS, INC.·00850021097554·

    Nu Skin Facial Spa

    FDA UDI
    NSE PRODUCTS, INC.·00860196000303·

    Nu Skin Conductive Gel

    FDA UDI
    NSE PRODUCTS, INC.·00860196000310·

    Nu Skin Facial Spa Package

    FDA UDI
    NSE PRODUCTS, INC.·00860196000327·

    AP 24® Smile Pop Toothbrush

    FDA UDI
    NSE PRODUCTS, INC.·00850021097578·

    NU SKIN CONDUCTIVE GEL

    FDA Adverse Event
    Injury ·NSE PRODUCTS, INC.·Product code GYB·June 16, 2025

    NU SKIN FACIAL SPA

    FDA Adverse Event
    Injury ·NSE PRODUCTS, INC.·Product code NFO·June 16, 2025

    CONDUCTIVE GEL

    FDA Adverse Event
    Injury ·NSE PRODUCTS, INC.·Product code GYB·March 18, 2021

    FACIAL SPA

    FDA Adverse Event
    Injury ·NSE PRODUCTS, INC.·Product code NFO·March 18, 2021

    Ultradent Products, Chromaclone PVS, Fast Set heavy body, Bubble Gum Flavor, 50 ml, Impression Material, Part No. 5013, Lot No. B7DS3, Used in prosthodontics.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code ELW·February 4, 2013

    Ultradent Products, Chromaclone PVS, Regular Set heavy body, Bubble Gum Flavor, 50 ml, Impression Material, Part No. 5012, Lot No. B7PPC. Used in prosthodontics.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code ELW·February 4, 2013

    Dental Explorer Single End #7, Mfr. Part Code/Product Code 100-7409. Distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B057701. The product is labeled in part, HENRY SCHEIN 100-7409 Explorer - Single End #7 SE. +H65810074090C. Made in China. For professional use only. Instruments must be cleaned and sterilized prior to use. Distributed by: HENRY SCHEIN, INC. 135 Duryea Road, Melville, NY 11747 USA. --- This product is a dental explorer made of stainless steel packaged individually within a sleeve and containing a cardboard insert (labeling).

    FDA Recall
    Terminated ·Hu-Friedy Mfg Co, Inc.·Product code EKB·January 7, 2005