FDA UDI In Commercial Distribution 🇺🇸 United States

iTero Lumina Pro

DI: 00816063022213 · Model: 221951 · Align Technology, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTero Lumina Pro
Primary DI
00816063022213
Version / Model
221951
Company Name
Align Technology, Inc.
Labeler DUNS
013831768
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-19
Public Version
1
Public Version Date
2024-11-27
Public Version Status
New
Public Device Record Key
7f04b4a3-de38-44db-af07-71d84420591b

Device Description

iTero Lumina Pro US Cart Configuration

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NTK Caries Detector, Laser Light, Transmission
QJK Intraoral Camera

GMDN Terms

Code Name
63669 Intraoral optical scanning system

Identifiers

Type ID
Primary 00816063022213

Premarket Submissions

Submission Number Supplement Number
K240573 000