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Cameo

FDA UDI

Class II (US FDA UDI)

by Aidite (Qinhuangdao) Technology Co., Ltd.

Identity

Trade Name
Cameo FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
Used for making all-porcelain restorations FDA UDI
Model / Reference
HT FDA UDI
Description
Used for making all-porcelain restorations FDA UDI

Identifiers

Primary DI / UDI-DI
06975164778291 FDA UDI
510(k) Number
K192231 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramic

Cameo by Aidite (Qinhuangdao) Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Cleared under the same submission

K192231 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aidite (Qinhuangdao) Technology Co., Ltd.

Sources (1)

  • FDA UDI 37cfb005-f62b-4224-a50a-7e3109fdb5b7 35 fields · synced May 30, 2026