# Adaptiiv

- Location (FDA's records): Halifax, CA
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: MUJ (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- 3D Bolus, Inc.: 1 (https://510kreport.com/company/3d-bolus)

## Firms that cite its devices most
- Adaptiiv Medical Technologies, Inc.: 2 (https://510kreport.com/company/adaptiiv-medical-technologies)

## Its most-cited devices
- K213438: 3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory (2022), cited by 2

## Recent decisions
- K213438: 3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory (Jan 19, 2022)

Source page: https://510kreport.com/company/adaptiiv