510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023671Substantially Equivalent

Aqueous Acrylic Dispersion 28% W/w

CHX Technologies Inc., Toronto, Ontario, CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K023671 is the FDA 510(k) clearance record for AQUEOUS ACRYLIC DISPERSION 28% W/W, a class II device, cleared for Chx Technologies, Inc. on under FDA product code LBH (Varnish, Cavity). FDA records list one 510(k) clearance for Chx Technologies, Inc. As of , FDA records show no recalls naming K023671.

Clearance record

Decision date
Received
(24 days to decision)
Product code
LBH Varnish, Cavity
Regulation
21 CFR 872.3260
Device class
Class II
Review panel
Dental
Applicant
Chx Technologies, Inc. 4800 Dundas St. W. Suite 105, Toronto, Ontario, CA
510(k) summary
Statement
Third party review
No

Clearances, product code LBH

Trailing 12 months
6 clearances under product code LBH in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LBH, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20261
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260