510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140894Substantially Equivalent

Argen Pmma

The Argen Corporation, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140894 is the FDA 510(k) clearance record for ARGEN PMMA, a class II device, cleared for The Argen Corporation on under FDA product code EBG (Crown And Bridge, Temporary, Resin). FDA records list 11 510(k) clearances for The Argen Corporation, from to . As of , FDA records show no recalls naming K140894.

Clearance record

Decision date
Received
(114 days to decision)
Product code
EBG Crown And Bridge, Temporary, Resin
Regulation
21 CFR 872.3770
Device class
Class II
Review panel
Dental
Applicant
The Argen Corporation 5855 Oberlin Dr., San Diego CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EBG

Trailing 12 months
2 clearances under product code EBG in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260