FDA applicant

Southwest Technologies, Inc.

Kansas City, MO5 decisions1987–20103 recalls

FDA records 5 decisions for Southwest Technologies, Inc. (Kansas City, MO) from 1987 to 2010: 5 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and IPM (Cover, Limb). Its devices cite 10 predicates, 3 of them its own earlier devices. 3 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, physical medicine panel, where it files most

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

FDA decisions per year

1in 2010

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2021

2007high 1 (2019) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Southwest Technologies, 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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Other applicant names beginning “Southwest”

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

Southwest Artificial Eyes, Inc. 2 Southwest Medical Mfg., Inc. 2 Southwest Ergonomics 1

Southwest Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

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 “Southwest”