510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K925579Substantially Equivalent

Verasoft Casting Alloy

Aalba Dent, Inc., Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925579 is the FDA 510(k) clearance record for VERASOFT CASTING ALLOY, a class II device, cleared for Aalba Dent, Inc. on under FDA product code EJH (Alloy, Metal, Base). FDA records list 27 510(k) clearances for Aalba Dent, Inc., from to . As of , FDA records show no recalls naming K925579.

Clearance record

Decision date
Received
(132 days to decision)
Product code
EJH Alloy, Metal, Base
Regulation
21 CFR 872.3710
Device class
Class II
Review panel
Dental
Applicant
Aalba Dent, Inc. 1819 So. May St., Chicago IL
510(k) summary
Statement
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