gudid
Primary ID: FA7-1400J
7LS (UDI FA7-1400J)
Manufactured by FKA DISTRIBUTING CO., LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 7LS - Primary ID FA7-1400J
Device Regulatory Overview
The 7LS (Model/Catalog Number: FA7-1400J) is a medical device manufactured by FKA DISTRIBUTING CO., LLC. This product is indexed under FDA Product Code / Category Classification NFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FA7-1400J
- Product Code / EMDN
- NFO
- Device Name
- ReSculpt Micro-Current & Light Therapy
- Database Sync Date
- 2026-08-09 09:00:32
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 7LS?
The registered manufacturer of record for 7LS is FKA DISTRIBUTING CO., LLC.
What is the Primary UDI-DI identifier for 7LS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FA7-1400J.
What classification code is assigned to this device?
This device is registered under product classification code NFO.
Similar Classification Devices (NFO)
Other Devices by FKA DISTRIBUTING CO., LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint