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iTero Lumina Pro Upgrade

FDA UDI

Class II (US FDA UDI)

by Align Technology, Inc.

Identity

Trade Name
iTero Lumina Pro Upgrade FDA UDI
Generic Name
Intraoral optical scanning system FDA UDI
Device Name
iTero Lumina Pro US upgrade from Lumina FDA UDI
Model / Reference
221950 FDA UDI
Description
iTero Lumina Pro US upgrade from Lumina FDA UDI

Identifiers

Primary DI / UDI-DI
00816063022466 FDA UDI
510(k) Number
K240573 FDA UDI
FDA Product Code
NTK FDA UDI
QJK FDA UDI
GMDN Term
Intraoral optical scanning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1745 FDA UDI
872.3661 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraoral optical scanning system

iTero Lumina Pro Upgrade by Align Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraoral optical scanning system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e6d61ec-2e7d-4c3b-9ac3-60c176374f10 34 fields · synced Jun 6, 2026