gudid Primary ID: 516-852

SONTEC JORDAN RING RETRACTOR FRAME (UDI 516-852)

Manufactured by SONTEC INSTRUMENTS, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SONTEC JORDAN RING RETRACTOR FRAME (Model/Catalog Number: 516-852) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification FFO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 516-852
Product Code / EMDN: FFO
Device Name: SONTEC JORDAN RING RETRACTOR FRAME SEGMENTED, SLOTTED
Database Sync Date: 2026-08-09 09:07:00

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 SONTEC JORDAN RING RETRACTOR FRAME?

The registered manufacturer of record for SONTEC JORDAN RING RETRACTOR FRAME is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for SONTEC JORDAN RING RETRACTOR FRAME?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 516-852.

What classification code is assigned to this device?

This device is registered under product classification code FFO.

Similar Classification Devices (FFO)

Other Devices by SONTEC INSTRUMENTS, INC.

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