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MiYO Esthetic System

FDA UDI

Class II (US FDA UDI)

by Jensen Industries, Inc.

Identity

Trade Name
MiYO Esthetic System FDA UDI
Generic Name
Dental porcelain/ceramic restoration kit FDA UDI
Model / Reference
MiYO Gingival Carnation Paste 4g FDA UDI

Identifiers

Catalog Number
0951 FDA UDI
Primary DI / UDI-DI
00817340025675 FDA UDI
510(k) Number
K111743 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental porcelain/ceramic restoration kit 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramicDental porcelain/ceramic restoration kit

MiYO Esthetic System by Jensen Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental porcelain/ceramic restoration kit.

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 fc4d3ba2-4f0f-49b5-b083-89859337e9ac 34 fields · synced Jun 8, 2026