FDA UDI In Commercial Distribution 🇺🇸 United States

Custom Night Guard

DI: 00860013500702 · Model: 1 · GrindGuard Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Custom Night Guard
Primary DI
00860013500702
Version / Model
1
Company Name
GrindGuard Inc.
Labeler DUNS
117870267
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-17
Public Version
3
Public Version Date
2026-03-06
Public Version Status
Update
Public Device Record Key
340ed36e-9173-4b97-9554-2a584e80bcef

Device Description

Custom Hybrid Night Guard

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MQC Mouthguard, Prescription
OBR Mouthguard, Over-The-Counter
OCO Mouthguard, Migraine/Tension Headache

GMDN Terms

Code Name
38620 Custom-made mouthguard

Identifiers

Type ID
Primary 00860013500702