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Coe Alginate™

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
COE ALGINATE™ FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
COE ALGINATE™ Normal set, mint, 5 x 5lb powder (25lb total) FDA UDI
Model / Reference
120025 FDA UDI
Description
COE ALGINATE™ Normal set, mint, 5 x 5lb powder (25lb total) FDA UDI

Identifiers

Catalog Number
120025 FDA UDI
Primary DI / UDI-DI
10386040004701 FDA UDI
D6581200251 FDA UDI
510(k) Number
K894282 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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: Silicone dental impression material

Coe Alginate™ by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

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 (2)

  • FDA UDI 2b7e20f1-cd97-418e-94bc-2e9c5fd804f8 38 fields · synced Jun 8, 2026
  • FDA UDI 9eaaebac-9c58-4815-8cc7-0eacdf07cfbe 38 fields · synced May 26, 2026