FDA applicant

Precept, Inc.

Mchenry, IL5 decisions1976–19770 recalls

FDA records 5 decisions for Precept, Inc. (Mchenry, IL) from 1976 to 1977: 5 510(k) clearances. Most are in product codes FXX (Mask, Surgical) and CAD (Vaporizer, Anesthesia, Non-Heated). 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 Precept, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precept, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Precept”

FDA records each applicant name separately; these may or may not be the same firm.

Precept Medical Products, Inc. 1

Precept, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Precept”