gudid Primary ID: 10203462.CGR

FOSTER GRANT (UDI 10203462.CGR)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The FOSTER GRANT (Model/Catalog Number: 10203462.CGR) is a medical device manufactured by FGX INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification HQY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10203462.CGR
Product Code / EMDN: HQY
Device Name
Database Sync Date: 2026-08-09 09:00:32

Full Regulatory Attributes

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{
    "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 FOSTER GRANT?

The registered manufacturer of record for FOSTER GRANT is FGX INTERNATIONAL INC..

What is the Primary UDI-DI identifier for FOSTER GRANT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10203462.CGR.

What classification code is assigned to this device?

This device is registered under product classification code HQY.

Similar Classification Devices (HQY)

Other Devices by FGX INTERNATIONAL INC.

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