510(k) Report

FDA applicant

Integrity Practice Management, Inc.

Sioux Falls, SD1 decision2002–20020 recalls

FDA records 1 decision for Integrity Practice Management, Inc. (Sioux Falls, SD) in 2002: 1 510(k) clearance. All are in product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided Integrity Practice Management, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Integrity Practice Management, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JAASystem, X-Ray, Fluoroscopic, Image-Intensified1decision

What has FDA decided for it lately?

  • K022911Model AMI1200 C-ArmIntegrity Practice Management, Inc. · 2002

The one decision as Integrity Practice Management, Inc. →

Other applicant names beginning “Integrity”

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

Integrity Implants, Inc. 11Integrity Spine 2Integrity Optics, Inc. 2Integrity Life Sciences 1Integrity Medical Software, Inc. 1Integrity Spine Lumbar Interbody Fusion System 1Integrity Implants Inc. Dba Accelus 1Integrity Orthopaedics, Inc. 1