510(k) Report

FDA applicant

Ipos KG

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Ipos KG (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code GBI (Material, External Aesthetic Restoration, Used…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Ipos KG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ipos KG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ipos KG 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.