gudid
Primary ID: 1
Dentemp SleepTight (UDI 1)
Manufactured by Doc Brands, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dentemp SleepTight - Primary ID 1
Device Regulatory Overview
The Dentemp SleepTight (Model/Catalog Number: 1) is a medical device manufactured by Doc Brands, Inc.. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- LRK
- Device Name
- Dentemp SleepTight in an OTC anti-snoring mouthpiece intended for use by adults as an aid to reduce snoring.
- Database Sync Date
- 2026-08-09 09:20:06
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 Dentemp SleepTight?
The registered manufacturer of record for Dentemp SleepTight is Doc Brands, Inc..
What is the Primary UDI-DI identifier for Dentemp SleepTight?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Doc Brands, Inc.
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