510(k) Report

FDA applicant

Aat Alber Antriebstechnik GmbH

Texas City, TX3 decisions2010–20150 recalls

FDA records 3 decisions for Aat Alber Antriebstechnik GmbH (Texas City, TX) from 2010 to 2015: 3 510(k) clearances. Most are in product codes ILK (Transport, Patient, Powered) and ITI (Wheelchair, Powered). Its devices cite 3 predicates, 1 of them its own earlier devices. 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 Aat Alber Antriebstechnik GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2010: 12014: 12015: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Aat Alber Antriebstechnik GmbH by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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