FDA applicant

Promident, LLC

New City, NY2 decisions2008–20170 recalls

FDA records 2 decisions for Promident, LLC (New City, NY) from 2008 to 2017: 2 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EBZ (Activator, Ultraviolet, For Polymerization). 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, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Promident, LLC by year, 2008–2026Sources: 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 Mfg., Ltd. 1

Promident, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Promident”