510(k) Report

FDA applicant

Natureplex, LLC

Olive Branch, MS2 decisions2005–20180 recalls

FDA records 2 decisions for Natureplex, LLC (Olive Branch, MS) from 2005 to 2018: 2 510(k) clearances. Most are in product codes NUC (Lubricant, Personal) and LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Natureplex, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2018: 1
2007high 1 (2018) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Natureplex, LLC’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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Which product codes does it file in?

  • NUCLubricant, Personal1decision
  • LCXKit, Test, Pregnancy, Hcg, Over The Counter1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K180828Natureplex Warm Touch Warming JellyNatureplex, LLC · 2018
  • K051963BE-Certain Pregnancy TestNatureplex, LLC · 2005

All 2 as Natureplex, LLC →