Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K130672Substantially Equivalent

Optiflow II Flowable Composite, Lc

Pac-Dent International, Inc., Walnut CA / Traditional, Substantially Equivalent

K130672 is the FDA 510(k) clearance record for OPTIFLOW II FLOWABLE COMPOSITE, LC, a class II device, cleared for Pac-Dent International, Inc. on under FDA product code EBF (Material, Tooth Shade, Resin). FDA records list 9 510(k) clearances for Pac-Dent International, Inc., from to . As of , FDA records show no recalls naming K130672.

Clearance record

Decision date
Received
(154 days to decision)
Product code
EBF Material, Tooth Shade, Resin
Regulation
21 CFR 872.3690
Device class
Class II
Review panel
Dental
Applicant
Pac-Dent International, Inc. 21038 Commerce Pt.e Dr., Walnut CA
510(k) summary
Summary PDF
Third party review
No

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