← Back to catalogue

iTero Element 5D Plus upgrade cart configuration

FDA UDI

Class II (US FDA UDI)

by Align Technology, Inc.

Identity

Trade Name
iTero Element 5D Plus upgrade cart configuration FDA UDI
Generic Name
Dental milling system, CAD/CAM, chairside FDA UDI
Device Name
Scanner, upgrade cart configuration FDA UDI
Model / Reference
211572 FDA UDI
Description
Scanner, upgrade cart configuration FDA UDI

Identifiers

Primary DI / UDI-DI
00816063020721 FDA UDI
510(k) Number
K193659 FDA UDI
FDA Product Code
NTK FDA UDI
GMDN Term
Dental milling system, CAD/CAM, chairside FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1745 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental milling system, CAD/CAM, chairside

iTero Element 5D Plus upgrade cart configuration by Align Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental milling system, CAD/CAM, chairside.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a1ea15d3-fe60-476a-9c07-50b284da4c3d 34 fields · synced May 29, 2026