FDA applicant

Ameriflo Corp.

Carmel, IN2 decisions2004–20060 recalls

FDA records 2 decisions for Ameriflo Corp. (Carmel, IN) from 2004 to 2006: 2 510(k) clearances. All are in product code NFB (Conserver, Oxygen). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Ameriflo Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ameriflo Corp.

Which product codes does it file in?

What has FDA decided for it lately?