Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K903009Substantially Equivalent

Argenco III

Argen Precious Metals, Inc., San Diego CA / Traditional, Substantially Equivalent

K903009 is the FDA 510(k) clearance record for ARGENCO III, a class II device, cleared for Argen Precious Metals, Inc. on under FDA product code EJS (Alloy, Other Noble Metal). FDA records list 217 510(k) clearances for Argen Precious Metals, Inc., from to . As of , FDA records show no recalls naming K903009.

Clearance record

Decision date
Received
(35 days to decision)
Product code
EJS Alloy, Other Noble Metal
Regulation
21 CFR 872.3060
Device class
Class II
Review panel
Dental
Applicant
Argen Precious Metals, Inc. 8380 Miralani Dr., San Diego CA
Third party review
No

Clearances, product code EJS

Trailing 12 months

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

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