FDA applicant

Interlectric Corp.

Warren, PA3 decisions1987–20150 recalls

FDA records 3 decisions for Interlectric Corp. (Warren, PA) from 1987 to 2015: 3 510(k) clearances. Most are in product codes LBI (Unit, Neonatal Phototherapy) and FTC (Light, Ultraviolet, Dermatological). No recall is linked to its devices.

FDA’s records also spell it “Interlectric Corporation”.

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 Interlectric Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Interlectric Corp.

Which product codes does it file in?

What has FDA decided for it lately?