UNI-FLEX RESIN— 510(k) K983461

Name: FDA 510(k) clearance K983461
Creator: U.S. Food and Drug Administration
Published: 1999-04-13

Substantially Equivalent

Trans-Atlantic Dental

FDA 510(k) clearance K983461 for UNI-FLEX RESIN, Substantially Equivalent on 1999-04-13. Applicant: Trans-Atlantic Dental. Device class: 2.

Clearance details

Applicant: Trans-Atlantic Dental
Product code: Code EBI
Device class: Class 2
Regulation: 21 CFR 872.3760
Advisory panel: Dental
Date received: 1998-10-01
Decision date: 1999-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Trenton, NJ, US

Download summary PDF View on FDA.gov ↗

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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.