# Orbbo Surgical, LLC

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 4 (2016–2017): 4 510(k) clearances
- Product codes: KWQ (1), ODP (1), MAX (1), NKB (1)
- 510(k) review time since 2016: median 55 days, against 87 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 4 (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
- Spineway: 2 (https://510kreport.com/company/spineway)
- Qualgenix: 1 (https://510kreport.com/company/qualgenix)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)

## Recent decisions
- K163265: Kepler II (Apr 7, 2017)
- K163602: Kepler I Cervical Plate System (Feb 16, 2017)
- K163566: Hubble I System (Feb 9, 2017)
- K163180: Hubble II (Dec 29, 2016)

Source page: https://510kreport.com/company/orbbo-surgical