FDA applicant

Stackhouse Assoc.

Riverside, CA5 decisions1979–199115 recalls

FDA records 5 decisions for Stackhouse Assoc. (Riverside, CA) from 1979 to 1991: 5 510(k) clearances. Most are in product codes FYD (Apparatus, Exhaust, Surgical) and FYA (Gown, Surgical). 15 recalls are 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 Stackhouse Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stackhouse Assoc. since 2007.

Recalls per year

13in 2015

2007high 13 (2015) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Stackhouse”

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

Stackhouse, Inc. 4

Stackhouse Assoc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Stackhouse”