# Adcura, Inc.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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
- Spineex, Inc.: 3 (https://510kreport.com/company/spineex)

## Recent decisions
- K223065: Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices (Oct 26, 2022)

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