FDA applicant

PolyConversions, Inc.

Champaign, IL3 decisions2023–20260 recalls

FDA records 3 decisions for PolyConversions, Inc. (Champaign, IL) from 2023 to 2026: 3 510(k) clearances. All are in product code QPC (Gown, Non-Sterile, Non-Isolation, Intended To…). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2025

2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — PolyConversions, Inc. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like PolyConversions, Inc.’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

PolyConversions, Inc.

Which product codes does it file in?

What has FDA decided for it lately?