gudid Primary ID: 20-0728

BSSO SPLITTING OSTEOTOME 1/6mm (UDI 20-0728)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BSSO SPLITTING OSTEOTOME 1/6mm (Model/Catalog Number: 20-0728) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification EMM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 20-0728
Product Code / EMDN: EMM
Device Name
Database Sync Date: 2026-08-09 09:01:17

Full Regulatory Attributes

🔒 Token Gated

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BSSO SPLITTING OSTEOTOME 1/6mm?

The registered manufacturer of record for BSSO SPLITTING OSTEOTOME 1/6mm is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for BSSO SPLITTING OSTEOTOME 1/6mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20-0728.

What classification code is assigned to this device?

This device is registered under product classification code EMM.

Similar Classification Devices (EMM)

Other Devices by W.H. Holden, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint