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Orchestrate 3D

FDA UDI

Class II (US FDA UDI)

by Orchestrate 3D

Identity

Trade Name
Orchestrate 3D FDA UDI
Generic Name
Dental milling system, CAD/CAM, chairside FDA UDI
Device Name
Orthodontic Software FDA UDI
Model / Reference
1 FDA UDI
Description
Orthodontic Software FDA UDI

Identifiers

Primary DI / UDI-DI
00860008123404 FDA UDI
510(k) Number
K181112 FDA UDI
FDA Product Code
PNN FDA UDI
GMDN Term
Dental milling system, CAD/CAM, chairside FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental milling system, CAD/CAM, chairside

Orchestrate 3D by Orchestrate 3D — 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

K181112 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orchestrate 3D

Sources (1)

  • FDA UDI 2654a873-7a10-4321-a149-60d6ffe9606b 34 fields · synced May 30, 2026