FDA UDI In Commercial Distribution 🇺🇸 United States

The Silencer

DI: 00810002220258 · Model: 3014680794 · JOHN'S DENTAL LABORATORY INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
The Silencer
Primary DI
00810002220258
Version / Model
3014680794
Company Name
JOHN'S DENTAL LABORATORY INC
Labeler DUNS
016649253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-03
Public Version
2
Public Version Date
2023-12-25
Public Version Status
Update
Public Device Record Key
fbee9d70-139a-44d4-bce8-eb39cc455890

Device Description

A removable intraoral device designed to treat mild - moderate sleep apnea and snoring. This is a reusable device.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
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 00810002220258