PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS— 510(k) K072572

Substantially Equivalent

Lifecore Biomedical, Inc.

FDA 510(k) clearance K072572 for PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS, Substantially Equivalent on 2007-10-05. Applicant: Lifecore Biomedical, Inc..

Clearance details

Applicant: Lifecore Biomedical, Inc.
Product code: Code NHA
Advisory panel: Dental
Date received: 2007-09-12
Decision date: 2007-10-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Chaska, MN, US

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Adverse events under product code NHA

product code NHA

Injury: 1,270
Malfunction: 2,860
Total: 4,130

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.