ANCHOR IIA/2 STAGE OSSEO. TIT. 6/4 ALLOY IMPLANT— 510(k) K871887

Substantially Equivalent

Anchor Implants , Ltd.

FDA 510(k) clearance K871887 for ANCHOR IIA/2 STAGE OSSEO. TIT. 6/4 ALLOY IMPLANT, Substantially Equivalent on 1987-07-31. Applicant: Anchor Implants , Ltd..

Clearance details

Applicant: Anchor Implants , Ltd.
Product code: Code DZE
Advisory panel: Dental
Date received: 1987-05-14
Decision date: 1987-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

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.