# Vertiflex (Tm), Incorporated

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 2 (2007–2007): 2 510(k) clearances
- Product codes: MQP (1), MNH (1)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stryker Spine: 2 (https://510kreport.com/company/stryker-spine)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)
- Quantum Orthopedics, Inc.: 1 (https://510kreport.com/company/quantum-orthopedics)
- Signus Medizintechnik GmbH: 1 (https://510kreport.com/company/signus-medizintechnik)
- Seaspine, Inc.: 1 (https://510kreport.com/company/seaspine)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)

## Firms that cite its devices most
- Vertiflex, Inc.: 3 (https://510kreport.com/company/vertiflex)
- Spine Wave, Inc.: 1 (https://510kreport.com/company/spine-wave)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)

## Its most-cited devices
- K062670: Vertiflex Spinal Screw System (2007), cited by 3
- K070218: Vertiflex Octane Peek Vertebral Body Replacement (Peek VBR) (2007), cited by 2

## Recent decisions
- K070218: Vertiflex Octane Peek Vertebral Body Replacement (Peek VBR) (Apr 6, 2007)
- K062670: Vertiflex Spinal Screw System (Jan 12, 2007)

Source page: https://510kreport.com/company/vertiflex-tm