TOKUSO REBASE— 510(k) K896981

Substantially Equivalent

Tokuyama America, Inc.

FDA 510(k) clearance K896981 for TOKUSO REBASE, Substantially Equivalent on 1990-05-15. Applicant: Tokuyama America, Inc..

Clearance details

Applicant: Tokuyama America, Inc.
Product code: Code EBI
Advisory panel: Dental
Date received: 1989-12-13
Decision date: 1990-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.