FDA applicant

Spartan Ultrasonics, Inc.

Fenton, MO2 decisions1999–20000 recalls

FDA records 2 decisions for Spartan Ultrasonics, Inc. (Fenton, MO) from 1999 to 2000: 2 510(k) clearances. Most are in product codes ELC (Scaler, Ultrasonic) and EJI (Syringe, Cartridge). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Spartan Ultrasonics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Spartan Ultrasonics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Spartan”

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

Spartan Micro, Inc. 4 Spartan Laboratories, Inc. 2 Spartan Healthcare Products Co. 2 Spartan Bioscience, Inc. 1 Spartan Marketing Group 1

Spartan Ultrasonics, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Spartan”