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EXAlence™

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
EXAlence™ FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
EXA’lence™ Putty, 500g (278mL) Base Jar, 500g (278mL) Catalyst Jar Clinic 5-5 Pack with accessories FDA UDI
Model / Reference
137405 FDA UDI
Description
EXA’lence™ Putty, 500g (278mL) Base Jar, 500g (278mL) Catalyst Jar Clinic 5-5 Pack with accessories FDA UDI

Identifiers

Catalog Number
137405 FDA UDI
Primary DI / UDI-DI
D6581374051 FDA UDI
510(k) Number
K043493 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

Category: Silicone dental impression material

EXAlence™ 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 (1)

  • FDA UDI e708a7fc-ea78-4956-88bb-f5dc92139495 37 fields · synced Jun 8, 2026