FLEXOR (DENTURE ACRYLIC RELINE MATERIAL)— 510(k) K902972

Substantially Equivalent

Cmp Industries, LLC

FDA 510(k) clearance K902972 for FLEXOR (DENTURE ACRYLIC RELINE MATERIAL), Substantially Equivalent on 1990-10-04. Applicant: Cmp Industries, LLC.

Clearance details

Applicant: Cmp Industries, LLC
Product code: Code EBI
Advisory panel: Dental
Date received: 1990-07-06
Decision date: 1990-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albany, NY, US

Download summary PDF View on FDA.gov ↗

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.