FDA applicant

Adaptive Switch Laboratories, Inc.

Houston, TX4 decisions1991–19920 recalls

FDA records 4 decisions for Adaptive Switch Laboratories, Inc. (Houston, TX) from 1991 to 1992: 4 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Adaptive Switch Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Adaptive Switch Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Adaptive”

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

Adaptive Video, Inc. 3 Adaptive Biotechnologies Corporation 2 Adaptive Specialty, LLC 2 Adaptive Healthcare Technologies, Inc. 1

Adaptive Switch Laboratories, Inc.

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?

Other applicant names beginning “Adaptive”