# Happe Spine

- Location (FDA's records): Grand Rapids, MI
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: ODP (1)
- Predicates its devices cite: 3 (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
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Zimmer Trabecular Metal Technology: 1 (https://510kreport.com/company/zimmer-trabecular-metal-technology)
- Spinefrontier, Inc.: 1 (https://510kreport.com/company/spinefrontier)

## Firms that cite its devices most
- Zsfab, Inc.: 1 (https://510kreport.com/company/zsfab)
- Ulrich Medical USA: 1 (https://510kreport.com/company/ulrich-medical-usa)

## Its most-cited devices
- K222004: INTEGRATE -C Interbody Fusion System (2023), cited by 2

## Recent decisions
- K222004: INTEGRATE -C Interbody Fusion System (Apr 28, 2023)

Source page: https://510kreport.com/company/happe-spine