FDA applicant

Kinetic Rehabilitation Instruments, Inc.

Washington, DC1 decision1996–19960 recalls

FDA records 1 decision for Kinetic Rehabilitation Instruments, Inc. (Washington, DC) in 1996: 1 510(k) clearance. 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 Kinetic Rehabilitation Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kinetic Rehabilitation Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kinetic Rehabilitation Instruments, 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 “Kinetic”

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

Kinetic Medical Products 63 Kinetic Concepts, Inc. 48 Kinetic Technology, Inc. 5 Kinetic Biomedical Services, Inc. 5 Kinetic Instruments, Inc. 2 Kinetic Surgical, LLC 2 Kinetic Resources, Inc. 1 Kinetic Innovative Seating System, LLC 1

Kinetic Rehabilitation Instruments, 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 “Kinetic”