HDC SPIDER SCREW— 510(k) K052471

Substantially Equivalent

Hdc S.R.L.

FDA 510(k) clearance K052471 for HDC SPIDER SCREW, Substantially Equivalent on 2005-12-23. Applicant: Hdc S.R.L..

Clearance details

Applicant: Hdc S.R.L.
Product code: Code DZE
Advisory panel: Dental
Date received: 2005-09-08
Decision date: 2005-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

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.