FDA applicant

Curon Medical, Inc.

Sunnyvale, CA3 decisions2000–20020 recalls

FDA records 3 decisions for Curon Medical, Inc. (Sunnyvale, CA) from 2000 to 2002: 3 510(k) clearances. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 10 predicates, 1 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 Curon Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Curon Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Curon Medical, 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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Other applicant names beginning “Curon”

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

Curon Scientific Co., Ltd. 1

Curon Medical, 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?

Other applicant names beginning “Curon”