FDA applicant

Instranetics, Inc.

Mchenry, IL10 decisions1977–19830 recalls

FDA records 10 decisions for Instranetics, Inc. (Mchenry, IL) from 1977 to 1983: 10 510(k) clearances. Most are in product codes KDC (Instrument, Surgical, Disposable) and HXB (Probe). 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 Instranetics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Instranetics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Instranetics, Inc.’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

Instranetics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?