FDA applicant
Motion Analysis Corp.
FDA records 4 decisions for Motion Analysis Corp. (Santa Rosa, CA) in 1989: 4 510(k) clearances. Most are in product codes LXJ (Interactive Rehabilitation Exercise Devices) and POV (Semen Analysis Device). 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 Motion Analysis Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Motion Analysis Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Motion Analysis Corp.’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 “Motion”
FDA records each applicant name separately; these may or may not be the same firm.