INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.— 510(k) K922872

Substantially Equivalent

Interpore Intl.

FDA 510(k) clearance K922872 for INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM., Substantially Equivalent on 1994-07-25. Applicant: Interpore Intl..

Clearance details

Applicant: Interpore Intl.
Product code: Code DZE
Advisory panel: Dental
Date received: 1992-06-15
Decision date: 1994-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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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.