FDA applicant

Pyramid Air Systems

Grainvalley, MO1 decision1997–19970 recalls

FDA records 1 decision for Pyramid Air Systems (Grainvalley, MO) in 1997: 1 510(k) clearance. All are in product code FYD (Apparatus, Exhaust, Surgical). 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 Pyramid Air Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pyramid Air Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pyramid Air Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Pyramid”

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

Pyramid Biological Corp. 12 Pyramid 2 Pyramid Medical, Inc. 1 Pyramid Handbags, Inc. 1

Pyramid Air Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pyramid”