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Nature-Cryl®

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
NATURE-CRYL® FDA UDI
Generic Name
Dental acrylic resin FDA UDI
Device Name
NATURE-CRYL® SUPER HI IMPACT MODERATE 5lb POWDER FDA UDI
Model / Reference
349818 FDA UDI
Description
NATURE-CRYL® SUPER HI IMPACT MODERATE 5lb POWDER FDA UDI

Identifiers

Catalog Number
349818 FDA UDI
Primary DI / UDI-DI
10386040008075 FDA UDI
510(k) Number
K051358 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental acrylic resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 5 Pound FDA UDI

Category: Dental acrylic resin

Nature-Cryl® by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental acrylic resin.

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 4a1ab1e6-6070-444d-8fe8-1f61b6db3ce2 38 fields · synced May 31, 2026