FDA applicant

Appian Medical, Inc.

Severna Park, MD1 decision2015–20150 recalls

FDA records 1 decision for Appian Medical, Inc. (Severna Park, MD) in 2015: 1 510(k) clearance. All are in product code MNR (Ventilatory Effort Recorder). 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 Appian Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Appian Medical, Inc. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Appian Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?