FDA applicant

Pollenex Corp.

Chicago, IL2 decisions1994–19940 recalls

FDA records 2 decisions for Pollenex Corp. (Chicago, IL) in 1994: 2 510(k) clearances. Most are in product codes ISA (Massager, Therapeutic, Electric) and FRF (Cleaner, Air, Medical Recirculating). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Pollenex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pollenex”

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

Pollenex Associated Mills, Inc. 4

Pollenex Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pollenex”