FDA applicant
Verticor, Ltd.
FDA records 3 decisions for Verticor, Ltd. (Round Rock, TX) from 2009 to 2011: 3 510(k) clearances. Most are in product codes KWQ (Appliance, Fixation, Spinal Intervertebral Body) and MQP (Spinal Vertebral Body Replacement Device). Its devices cite 10 predicates, 0 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 Verticor, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2009.
Planning a device like Verticor, Ltd.’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) Report