FDA applicant

Molecular Products, Ltd.

Bonita Springs, FL4 decisions1992–20240 recalls

FDA records 4 decisions for Molecular Products, Ltd. (Bonita Springs, FL) from 1992 to 2024: 4 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and CBL (Absorbent, Carbon-Dioxide). Its devices cite 3 predicates, 2 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, anesthesiology panel, where it files most

How often FDA has decided Molecular Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Molecular Products, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Molecular”

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

Molecular Biosystems, Inc. 4 Molecular Devices Corp. 4 Molecular Diagnostics 1 Molecular Matrix, Inc. 1 Molecular Technologies Corp. 1

Molecular Products, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Molecular”