Vitique 213055

by DMG Chemisch-Pharmazeutische Fabrik GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberEDMG2130551 UDI-DI	Date22 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Vitique
Generic Name: Dental composite resin
Model / Ref / Catalog: 213055

Primary DI / UDI-DI: EDMG2130551
510(k) Number: K023649
FDA Product Code: EMA
GMDN Term: Dental composite resin

Device Class: Class II
Regulation Number: 872.3275
GUDID distribution status: In Commercial Distribution

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Properties

Prescription Use
Lot / Batch Number
Serial 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
Premarket Exempt: No
Manufacturing Date: No