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DenFil Flow

VERICOM CO., LTD. · Model FR102-RA33 · UDI-DI 08809254451024

EBF Prescription
10
510(k) clearances
961
Adverse events (1 deaths)
71
Recalls
207
Facilities

Description

Light-Cured Radiopaque Flowable Composite Resin ; DenFil Flow A3 2g x 1 syringe

Recalls

DateFirmReason
2026-07-09Henry Schein Inc.Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
2026-07-09Henry Schein Inc.Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2020-08-31Ultradent Products, Inc.Due to a potential manufacturing issue (cross contamination), composite is non-homogeneous.
2019-07-09Voco GmbHThe metal cannula are potentially too loose and may become loose when applying the filing material.
2019-01-31RHONDIUM LIMITEDThe product was mislabeled with an incorrect expiration date.
2017-08-03Ivoclar Vivadent, Inc.Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing
2017-08-03Ivoclar Vivadent, Inc.Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.