FDA applicant

Promident Mfg., Ltd.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Promident Mfg., Ltd. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code EFB (Handpiece, Air-Powered, 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 Promident Mfg., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Promident Mfg., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Promident”

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

Promident, LLC 2

Promident Mfg., Ltd.

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 “Promident”