← Back to catalogue

Gc Occlusal Matrix System

FDA UDI

Class I (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
GC OCCLUSAL MATRIX SYSTEM FDA UDI
Generic Name
Dental impression spacer FDA UDI
Device Name
GC OCCLUSAL MATRIX SYSTEM Standard Package, Contains: 25 individual right & left quadrants FDA UDI
Model / Reference
439154 FDA UDI
Description
GC OCCLUSAL MATRIX SYSTEM Standard Package, Contains: 25 individual right & left quadrants FDA UDI

Identifiers

Catalog Number
439154 FDA UDI
Primary DI / UDI-DI
D6584391541 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental impression spacer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental impression spacer

Gc Occlusal Matrix System by Gc America Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression spacer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 5371beed-b536-42af-8842-d8987f937edf 35 fields · synced May 30, 2026