FDA applicant

Ascep, Inc.

Mchenry, IL9 decisions1979–19830 recalls

FDA records 9 decisions for Ascep, Inc. (Mchenry, IL) from 1979 to 1983: 9 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) 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 Ascep, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ascep, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ascep, Inc.

Which product codes does it file in?

What has FDA decided for it lately?