FDA applicant
Otto Bock Orthopedic Industry, Inc.
FDA records 6 decisions for Otto Bock Orthopedic Industry, Inc. (Plymouth, MN) from 1995 to 2000: 6 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and ITI (Wheelchair, Powered). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Otto Bock Orthopedic Industry, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Otto Bock Orthopedic Industry, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Otto Bock Orthopedic Industry, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Otto”
FDA records each applicant name separately; these may or may not be the same firm.