510(k) Report

FDA applicant

Med-Tech Rubber & Engineering Industries

Bombay, IN3 decisions1989–19960 recalls

FDA records 3 decisions for Med-Tech Rubber & Engineering Industries (Bombay, IN) from 1989 to 1996: 3 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and KGO (Surgeon'S Gloves). 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 Med-Tech Rubber & Engineering Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-Tech Rubber & Engineering Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Med-Tech Rubber & Engineering Industries by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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