FDA applicant

Jain Surgical Equipment, Inc.

Kalamazoo, MI5 decisions1990–19920 recalls

FDA records 5 decisions for Jain Surgical Equipment, Inc. (Kalamazoo, MI) from 1990 to 1992: 5 510(k) clearances. Most are in product codes MMK (Container, Sharps) and MDM (Instrument, Manual, Surgical, General Use). 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 hospital panel, where it files most

How often FDA has decided Jain Surgical Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jain Surgical Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Jain Surgical Equipment, Inc.

Which product codes does it file in?

What has FDA decided for it lately?