MODIFIED VINYLAC PRESS PACK DENTURE RESIN— 510(k) K864757

Substantially Equivalent

Astron Dental Corp.

FDA 510(k) clearance K864757 for MODIFIED VINYLAC PRESS PACK DENTURE RESIN, Substantially Equivalent on 1987-02-10. Applicant: Astron Dental Corp..

Clearance details

Applicant: Astron Dental Corp.
Product code: Code EBI
Advisory panel: Dental
Date received: 1986-12-05
Decision date: 1987-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

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Adverse events under product code EBI

product code EBI

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.