FDA applicant

Manan Manufacturing Co., Inc.

Skokie, IL20 decisions1985–19870 recalls

FDA records 20 decisions for Manan Manufacturing Co., Inc. (Skokie, IL) from 1985 to 1987: 20 510(k) clearances. Most are in product codes KNW (Instrument, Biopsy) and GAA (Needle, Aspiration And Injection, Disposable). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Manan Manufacturing Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Manan Manufacturing Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Manan Manufacturing Co., 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 “Manan”

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

Manan Medical Products, Inc. 39 Manan Medical Devices 1

Manan Manufacturing Co., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Manan”