FDA applicant
Quantum Orthopedics, Inc.
FDA records 6 decisions for Quantum Orthopedics, Inc. (Carlsbad, CA) from 2004 to 2006: 6 510(k) clearances. Most are in product codes MQP (Spinal Vertebral Body Replacement Device) and JDK (Prosthesis, Hip, Cement Restrictor). Its devices cite 6 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Quantum Orthopedics”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Quantum Orthopedics, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Quantum Orthopedics, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Quantum Orthopedics, 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 “Quantum”
FDA records each applicant name separately; these may or may not be the same firm.