FDA applicant

Carticept Medical, Inc.

Alpharetta, GA6 decisions2011–20150 recalls

FDA records 6 decisions for Carticept Medical, Inc. (Alpharetta, GA) from 2011 to 2015: 6 510(k) clearances. All are in product code FRN (Pump, Infusion). Its devices cite 8 predicates, 5 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 hospital panel, where it files most

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

FDA decisions per year

1in 2015

2011high 2 (2011) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Carticept Medical, Inc. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Carticept 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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Carticept Medical, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?