gudid
Primary ID: LXPOOFB
reVive Light Therapy (UDI LXPOOFB)
Manufactured by LED TECHNOLOGIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for reVive Light Therapy - Primary ID LXPOOFB
Device Regulatory Overview
The reVive Light Therapy (Model/Catalog Number: LXPOOFB) is a medical device manufactured by LED TECHNOLOGIES INC. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LXPOOFB
- Product Code / EMDN
- OLP
- Device Name
- Database Sync Date
- 2026-08-09 09:18:06
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 reVive Light Therapy?
The registered manufacturer of record for reVive Light Therapy is LED TECHNOLOGIES INC.
What is the Primary UDI-DI identifier for reVive Light Therapy?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LXPOOFB.
What classification code is assigned to this device?
This device is registered under product classification code OLP.
Similar Classification Devices (OLP)
Other Devices by LED TECHNOLOGIES INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint