510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832662Substantially Equivalent

Dental Syringe System-Various Styles

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

K832662 is the FDA 510(k) clearance record for DENTAL SYRINGE SYSTEM-VARIOUS STYLES, a class I device, cleared for Centrix, Inc. on under FDA product code KXR (Applicator, Resin). FDA records list 47 510(k) clearances for Centrix, Inc., from to . As of , FDA records show no recalls naming K832662.

Clearance record

Decision date
Received
(57 days to decision)
Product code
KXR Applicator, Resin
Regulation
21 CFR 872.3140
Device class
Class I
Review panel
Dental
Applicant
Centrix, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KXR

Trailing 12 months

FDA records hold no clearances under product code KXR in the trailing twelve months.

FDA records show no clearances under product code KXR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KXR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260