FDA UDI In Commercial Distribution 🇺🇸 United States

Reveal® Aligners

DI: 00190707090708 · Model: 572-2539 · ORTHO ORGANIZERS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reveal® Aligners
Primary DI
00190707090708
Version / Model
572-2539
Company Name
ORTHO ORGANIZERS, INC.
Labeler DUNS
062165188
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-14
Public Version
1
Public Version Date
2021-07-22
Public Version Status
New
Public Device Record Key
68f14e2d-5a39-4b80-9f5c-5cbebd1c67e2

Device Description

Reveal® Aligners - Refinements (1)

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NXC Aligner, sequential

GMDN Terms

Code Name
44738 Orthodontic progressive aligner

Identifiers

Type ID
Primary 00190707090708