FDA applicant

Vertiflex (Tm), Incorporated

Carlsbad, CA2 decisions2007–20070 recalls

FDA records 2 decisions for Vertiflex (Tm), Incorporated (Carlsbad, CA) in 2007: 2 510(k) clearances. Most are in product codes MQP (Spinal Vertebral Body Replacement Device) and MNH (Orthosis, Spondylolisthesis Spinal Fixation). Its devices cite 12 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, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Vertiflex (Tm), Incorporated’s devices, and how often a recall has named them.

FDA decisions per year

2in 2007

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vertiflex (Tm), Incorporated by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vertiflex (Tm), Incorporated’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

Other applicant names beginning “Vertiflex”

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

Vertiflex, Inc. 5

Vertiflex (Tm), Incorporated

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Vertiflex”