Medical Device
Manufacturing
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K233596Substantially Equivalent

VarseoSmile TriniQ

Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG, Bremen, DE / Traditional, Substantially Equivalent

K233596 is the FDA 510(k) clearance record for VarseoSmile TriniQ, a class II device, cleared for Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG on under FDA product code EBF (Material, Tooth Shade, Resin). FDA records list 3 510(k) clearances for Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG, from to . As of , FDA records show no recalls naming K233596.

Clearance record

Decision date
Received
(1 day to decision)
Product code
EBF Material, Tooth Shade, Resin
Regulation
21 CFR 872.3690
Device class
Class II
Review panel
Dental
Applicant
Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG Wilhelm-Herbst-Straße 1, Bremen, DE
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code EBF

Trailing 12 months
19 clearances under product code EBF in the twelve months to October 2026, April 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code EBF, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20262
April 20265
May 20262
June 20262
July 20262
August 20261
September 20262
October 20260