gudid Primary ID: 600-050

Orthosil (UDI 600-050)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Orthosil (Model/Catalog Number: 600-050) is a medical device manufactured by Ortho Organizers, Inc.. This product is indexed under FDA Product Code / Category Classification EGD within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 2 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2477-2020 View Full Alert →

Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484...

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-2478-2020 View Full Alert →

Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic Bracket REF711-299MCQ...

🔒 Compromised Lot & Serial Numbers Locked

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Unlock Lot Data ($49)

Technical Specifications

Model Number: 600-050
Product Code / EMDN: EGD
Device Name: Relief Silicone 50/pk
Database Sync Date: 2026-08-09 09:00:52

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 Orthosil?

The registered manufacturer of record for Orthosil is Ortho Organizers, Inc..

What is the Primary UDI-DI identifier for Orthosil?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 600-050.

What classification code is assigned to this device?

This device is registered under product classification code EGD.

Similar Classification Devices (EGD)

Other Devices by Ortho Organizers, Inc.

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