510(k) Report

FDA applicant

Intl. Equipment and Supply Corp.

Indianapolis, IN1 decision1990–19900 recalls

FDA records 1 decision for Intl. Equipment and Supply Corp. (Indianapolis, IN) in 1990: 1 510(k) clearance. All are in product code EIK (Carver, Wax, Dental). 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, dental panel, where it files most

How often FDA has decided Intl. Equipment and Supply Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intl. Equipment and Supply Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intl. Equipment and Supply Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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