FDA UDI In Commercial Distribution 🇺🇸 United States

Dentemp SleepTight

DI: 00372494103452 · Model: 1 · Doc Brands, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dentemp SleepTight
Primary DI
00372494103452
Version / Model
1
Company Name
Doc Brands, Inc.
Labeler DUNS
081254601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-03
Public Version
1
Public Version Date
2023-01-11
Public Version Status
New
Public Device Record Key
fbd73850-2bbe-4375-8f41-68224062dfa7

Device Description

Dentemp SleepTight in an OTC anti-snoring mouthpiece intended for use by adults as an aid to reduce snoring.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00372494103452

Customer Contacts

Phone
833-362-2763

Premarket Submissions

Submission Number Supplement Number
K191618 000