510(k) Report

FDA applicant

Oxy2plus, LLC

Rosemead, CA1 decision2021–20210 recalls

FDA records 1 decision for Oxy2plus, LLC (Rosemead, CA) in 2021: 1 510(k) clearance. All are in product code LFD (Saliva, Artificial). Its devices cite 1 predicate, 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

How often FDA has decided Oxy2plus, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Oxy2plus, LLC by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LFDSaliva, Artificial1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K202689Dentilube SprayOxy2plus, LLC · 2021

The one decision as Oxy2plus, LLC →