FDA applicant

Med-Plastics Intl., Inc.

Indianapolis, IN17 decisions1993–19950 recalls

FDA records 17 decisions for Med-Plastics Intl., Inc. (Indianapolis, IN) from 1993 to 1995: 17 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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, anesthesiology panel, where it files most

How often FDA has decided Med-Plastics Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-Plastics Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Med-Plastics Intl., 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?