510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864757Substantially Equivalent

Modified Vinylac Press Pack Denture Resin

Astron Dental Corporation, Wheeling IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864757 is the FDA 510(k) clearance record for MODIFIED VINYLAC PRESS PACK DENTURE RESIN, a class II device, cleared for Astron Dental Corp. on under FDA product code EBI (Resin, Denture, Relining, Repairing, Rebasing). FDA records list 6 510(k) clearances for Astron Dental Corp., from to . As of , FDA records show no recalls naming K864757.

Clearance record

Decision date
Received
(67 days to decision)
Product code
EBI Resin, Denture, Relining, Repairing, Rebasing
Regulation
21 CFR 872.3760
Device class
Class II
Review panel
Dental
Applicant
Astron Dental Corp. 280 Holdbrook Dr., Wheeling IL
Third party review
No

Clearances, product code EBI

Trailing 12 months
10 clearances under product code EBI in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EBI, trailing twelve months
MonthClearances
November 20253
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20263
August 20262
September 20260
October 20260