gudid
Primary ID: Snore Aid
SleepRight (UDI Snore Aid)
Manufactured by Splintek Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SleepRight - Primary ID Snore Aid
Device Regulatory Overview
The SleepRight (Model/Catalog Number: Snore Aid) is a medical device manufactured by Splintek Inc.. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Snore Aid
- Product Code / EMDN
- LRK
- Device Name
- SleepRight Snore Aid is intended for use by adult patients 18 years of age or older as an aid for the reduction of snoring.
- Database Sync Date
- 2026-08-09 09:04:20
Full Regulatory Attributes
🔒 Token Gated
{
"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 SleepRight?
The registered manufacturer of record for SleepRight is Splintek Inc..
What is the Primary UDI-DI identifier for SleepRight?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Snore Aid.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Splintek Inc.
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