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Shining 3d®

FDA UDI

Class I (US FDA UDI)

by Shining 3D Tech Co., Ltd.

Identity

Trade Name
SHINING 3D® FDA UDI
Generic Name
Jaw physiology evaluation system FDA UDI
Device Name
The product uses optical scanning method to collect facial 3D data and jaw movement tracking data to provide 3D digital models for facial and oral CAD design. FDA UDI
Model / Reference
MetiSmile FDA UDI
Description
The product uses optical scanning method to collect facial 3D data and jaw movement tracking data to provide 3D digital models for facial and oral CAD design. FDA UDI

Identifiers

Primary DI / UDI-DI
06970163085968 FDA UDI
FDA Product Code
NFS FDA UDI
GMDN Term
Jaw physiology evaluation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.2060 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Jaw physiology evaluation system

Shining 3d® by Shining 3D Tech Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Jaw physiology evaluation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f158f7c9-c8e7-4a1b-8df0-41da72d50d53 33 fields · synced Jun 1, 2026