FDA applicant
Aat Alber Antriebstechnik GmbH
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
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
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Aat Alber Antriebstechnik GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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