Osteotome (UDI HWM)
Device Regulatory Overview
The Osteotome (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification HWM within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- HWM
- Device Name
- Osteotome
- Database Sync Date
- 2026-08-09 09:00:27
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Osteotome?
The registered manufacturer of record for Osteotome is .
What is the Primary UDI-DI identifier for Osteotome?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HWM.
What classification code is assigned to this device?
This device is registered under product classification code HWM.
Programmatic Export
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JSON API Endpoint