FDA applicant

Optim, LLC

Sturbridge, MA6 decisions2008–20260 recalls

FDA records 6 decisions for Optim, LLC (Sturbridge, MA) from 2008 to 2026: 6 510(k) clearances. Most are in product codes EOB (Nasopharyngoscope (Flexible Or Rigid)) and FEH (Electrode, Flexible Suction Coagulator). Its devices cite 11 predicates, 3 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Optim, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

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

FDA decisions per year

1in 2021

2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Optim, LLC by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Optim, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?