# Safeop Surgical, Inc.

- Location (FDA's records): Hunt Valley, MD
- FDA decisions: 2 (2014–2019): 2 510(k) clearances
- Product codes: GWF (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 4 (1 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
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)
- Axon Systems, Inc.: 1 (https://510kreport.com/company/axon-systems)
- Nihon Kohden Corporation: 1 (https://510kreport.com/company/nihon-kohden)
- Cadwell Industries, Inc.: 1 (https://510kreport.com/company/cadwell-industries)
- Natus Medical, Inc.: 1 (https://510kreport.com/company/natus-medical)
- Strohl Medical Technologies: 1 (https://510kreport.com/company/strohl-medical-technologies)

## Firms that cite its devices most
- Alphatec Spine, Inc.: 2 (https://510kreport.com/company/alphatec-spine)
- Time IS Brain, S.L.: 1 (https://510kreport.com/company/time-is-brain)

## Its most-cited devices
- K182542: The EPAD 2 System (2019), cited by 2
- K132616: EPAD (2014), cited by 2

## Recent decisions
- K182542: The EPAD 2 System (Feb 22, 2019)
- K132616: EPAD (Jan 24, 2014)

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