FDA applicant

Pollux Endoscopy, Inc.

Sunrise, FL4 decisions1995–20000 recalls

FDA records 4 decisions for Pollux Endoscopy, Inc. (Sunrise, FL) from 1995 to 2000: 4 510(k) clearances. Most are in product codes HRX (Arthroscope) and FAJ (Cystoscope And Accessories, Flexible/Rigid). 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

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Pollux Endoscopy, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pollux Endoscopy, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pollux Endoscopy, Inc.

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?