Virtuoso® 032381835

by Den-Mat Holdings, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberD8130323818351 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Virtuoso®
Generic Name: Dental composite resin
Model / Ref / Catalog: 032381835

Primary DI / UDI-DI: D8130323818351
FDA Product Code: EBF
GMDN Term: Dental composite resin

Device Class: Class II
Regulation Number: 872.3690
GUDID distribution status: In Commercial Distribution

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Manufacturing Date: No