510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K911323Substantially Equivalent

Flux-N-All

Precident Corp., Glenview IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911323 is the FDA 510(k) clearance record for FLUX-N-ALL, a class II device, cleared for Precident Corp. on under FDA product code EJH (Alloy, Metal, Base). FDA records list 2 510(k) clearances for Precident Corp., from to . As of , FDA records show no recalls naming K911323.

Clearance record

Decision date
Received
(189 days to decision)
Product code
EJH Alloy, Metal, Base
Regulation
21 CFR 872.3710
Device class
Class II
Review panel
Dental
Applicant
Precident Corp. 3829 Harvest Ln., Glenview IL
Third party review
No

Clearances, product code EJH

Trailing 12 months

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

FDA records show no clearances under product code EJH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EJH, 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