gudid
Primary ID: 39-SF-5530
Reform Ti Modular (UDI 39-SF-5530)
Manufactured by PRECISION SPINE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reform Ti Modular - Primary ID 39-SF-5530
Device Regulatory Overview
The Reform Ti Modular (Model/Catalog Number: 39-SF-5530) is a medical device manufactured by PRECISION SPINE, INC.. This product is indexed under FDA Product Code / Category Classification NKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 39-SF-5530
- Product Code / EMDN
- NKB
- Device Name
- Modular Fenestrated Bone-Screw - 5.5 mm x 30 mm
- Database Sync Date
- 2026-08-09 09:33:11
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 Reform Ti Modular?
The registered manufacturer of record for Reform Ti Modular is PRECISION SPINE, INC..
What is the Primary UDI-DI identifier for Reform Ti Modular?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 39-SF-5530.
What classification code is assigned to this device?
This device is registered under product classification code NKB.
Similar Classification Devices (NKB)
Other Devices by PRECISION SPINE, INC.
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