Footshell Forever R24 Black - I.D. 210mm (UDI 05715763006668)
Manufactured by Levitate Technology ApS
Device Regulatory Overview
The Footshell Forever R24 Black - I.D. 210mm (Model/Catalog Number: LTA110006) is a medical device manufactured by Levitate Technology ApS. This product is indexed under FDA Product Code / Category Classification Y062499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LTA110006
- Product Code / EMDN
- Y062499
- Device Name
- Artificial Limb Components
- Database Sync Date
- 2026-08-09 16:48:59
Full Regulatory Attributes
๐ 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 Footshell Forever R24 Black - I.D. 210mm?
The registered manufacturer of record for Footshell Forever R24 Black - I.D. 210mm is Levitate Technology ApS.
What is the Primary UDI-DI identifier for Footshell Forever R24 Black - I.D. 210mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05715763006668.
What classification code is assigned to this device?
This device is registered under product classification code Y062499.
Similar Classification Devices (Y062499)
Other Devices by Levitate Technology ApS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint