FDA applicant

Laivan Corp.

East Rockaway, NY6 decisions1988–19930 recalls

FDA records 6 decisions for Laivan Corp. (East Rockaway, NY) from 1988 to 1993: 6 510(k) clearances. Most are in product codes NAD (Dressing, Wound, Occlusive) and KGX (Tape And Bandage, Adhesive). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Laivan Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laivan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Laivan Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Laivan Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Laivan Corp.

Which product codes does it file in?

What has FDA decided for it lately?