FDA applicant

Otto Bock Orthopaedische Industrie, Kg.

Minneapolis, MN1 decision2000–20000 recalls

FDA records 1 decision for Otto Bock Orthopaedische Industrie, Kg. (Minneapolis, MN) in 2000: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 Otto Bock Orthopaedische Industrie, Kg.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Otto Bock Orthopaedische Industrie, Kg. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Otto Bock Orthopaedische Industrie, 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 “Otto”

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

Otto Bock Healthcare LP 17 Otto Bock Orthopedic Industry, Inc. 6 Otto Bock Healthcare Products GmbH 3 Otto Bock, Austria GmbH 2 Otto Bock Pur Life Science GmbH 1 Otto Back Healthcare, LP 1 Otto C. Watzka 1

Otto Bock Orthopaedische Industrie, Kg.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Otto”