FDA applicant

Circon Corp.

Santa Barbara, CA6 decisions1997–19990 recalls

FDA records 6 decisions for Circon Corp. (Santa Barbara, CA) from 1997 to 1999: 6 510(k) clearances. Most are in product codes KNY (Accessories, Catheter, G-U) and KNF (Coagulator-Cutter, Endoscopic, Unipolar (And…). Its devices cite 6 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Circon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Circon Corp.’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 “Circon”

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

Circon Video 14 Circon Acmi 10

Circon Corp.

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 “Circon”