510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981972Substantially Equivalent

Green-or Dentin Desensitizer

Centrix, Inc., Shelton CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981972 is the FDA 510(k) clearance record for GREEN-OR DENTIN DESENSITIZER, a class II device, cleared for Centrix, Inc. on under FDA product code LBH (Varnish, Cavity). FDA records list 47 510(k) clearances for Centrix, Inc., from to . As of , FDA records show no recalls naming K981972.

Clearance record

Decision date
Received
(186 days to decision)
Product code
LBH Varnish, Cavity
Regulation
21 CFR 872.3260
Device class
Class II
Review panel
Dental
Applicant
Centrix, Inc. 770 River Rd., Shelton CT
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