510(k) Report

FDA applicant

Ipos Luneburg

Mchenry, IL8 decisions1980–19840 recalls

FDA records 8 decisions for Ipos Luneburg (Mchenry, IL) from 1980 to 1984: 8 510(k) clearances. Most are in product codes KNP (Orthosis, Corrective Shoe) and IQI (Orthosis, Limb Brace). 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 Ipos Luneburg’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ipos Luneburg since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ipos”

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