FDA applicant

Clareblend, Inc.

Elgin, IL3 decisions1988–20080 recalls

FDA records 3 decisions for Clareblend, Inc. (Elgin, IL) from 1988 to 2008: 3 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and KCW (Epilator, High Frequency, Needle-Type). Its devices cite 6 predicates, 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

2in 2008

2007high 2 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Clareblend, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?