NANCY NAIL— 510(k) K960642

Substantially Equivalent

Landos, Inc.

FDA 510(k) clearance K960642 for NANCY NAIL, Substantially Equivalent on 1996-05-17. Applicant: Landos, Inc..

Clearance details

Applicant: Landos, Inc.
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 1996-02-14
Decision date: 1996-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Malvern, PA, US

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.