GUDIDData
gudid Primary ID: 61020117

Colgate Optic White Professional In Office Whitening Kit (UDI 61020117)

Manufactured by COLGATE ORAL PHARMACEUTICALS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Colgate Optic White Professional In Office Whitening Kit - Primary ID 61020117

Device Regulatory Overview

The Colgate Optic White Professional In Office Whitening Kit (Model/Catalog Number: 61020117) is a medical device manufactured by COLGATE ORAL PHARMACEUTICALS, INC.. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
61020117
Product Code / EMDN
EEG
Device Name
Colgate Optic White Professional features a synergistic combination of a quick-dry whitening serum and a rechargeable LED whitening device. The serum, once applied with the precision brush, quickly forms a smudge-proof, concentrated hydrogen peroxide film on the patient's teeth. The LED device then uses the light energy to amplify the whitening power of the concentrated film even further.
Database Sync Date
2026-08-09 09:33:17

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Colgate Optic White Professional In Office Whitening Kit?

The registered manufacturer of record for Colgate Optic White Professional In Office Whitening Kit is COLGATE ORAL PHARMACEUTICALS, INC..

What is the Primary UDI-DI identifier for Colgate Optic White Professional In Office Whitening Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 61020117.

What classification code is assigned to this device?

This device is registered under product classification code EEG.

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