FDA applicant

Sparta Instrument Corp.

Mchenry, IL4 decisions1978–19860 recalls

FDA records 4 decisions for Sparta Instrument Corp. (Mchenry, IL) from 1978 to 1986: 4 510(k) clearances. Most are in product codes HAW (Neurological Stereotaxic Instrument) and KTI (Bronchoscope Accessory). 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, neurology panel, where it files most

How often FDA has decided Sparta Instrument Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sparta Instrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sparta”

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

Sparta Surgical Corp. 7 Sparta East, LLC 1

Sparta Instrument Corp.

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 “Sparta”