MEDICAL INTERPOROUS— 510(k) K051342

Substantially Equivalent

Bonyf AG

FDA 510(k) clearance K051342 for MEDICAL INTERPOROUS, Substantially Equivalent on 2006-06-02. Applicant: Bonyf AG.

Clearance details

Applicant: Bonyf AG
Product code: Code EFT
Advisory panel: Dental
Date received: 2005-05-23
Decision date: 2006-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Silver Creek, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EFT

product code EFT

Death: 8
Injury: 267
Total: 275

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.