510(k) Report

FDA applicant

Medical Alignment Systems

Sandy, UT3 decisions1987–19920 recalls

FDA records 3 decisions for Medical Alignment Systems (Sandy, UT) from 1987 to 1992: 3 510(k) clearances. Most are in product codes IWE (Monitor, Patient Position, Light-Beam) and INE (Sling, Overhead Suspension, Wheelchair). 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 Medical Alignment Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Alignment Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Alignment Systems 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?

  • IWEMonitor, Patient Position, Light-Beam2decisions
  • INESling, Overhead Suspension, Wheelchair1decision

What has FDA decided for it lately?

  • K923619Acculite SSLMedical Alignment Systems · 1992
  • K884787Acculite-PPL 5Medical Alignment Systems · 1989
  • K872841AcculiteMedical Alignment Systems · 1987

All 3 as Medical Alignment Systems →