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Miracle Mix®

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
Miracle Mix® FDA UDI
Generic Name
Glass ionomer dental cement FDA UDI
Device Name
Miracle Mix® Capsules (48) FDA UDI
Model / Reference
452100 FDA UDI
Description
Miracle Mix® Capsules (48) FDA UDI

Identifiers

Catalog Number
452100 FDA UDI
Primary DI / UDI-DI
D6584521001 FDA UDI
510(k) Number
K981370 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Glass ionomer dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glass ionomer dental cement

Miracle Mix® by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glass ionomer dental cement.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 17f3541c-6f1b-4db2-9e32-3631d7f221ce 37 fields · synced Jun 8, 2026