# Thompson Mis, Inc.

- Location (FDA's records): Salem, NH
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Difusion Technologies: 1 (https://510kreport.com/company/difusion-technologies)
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Kiscomedica S.A.: 1 (https://510kreport.com/company/kiscomedica)

## Firms that cite its devices most
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)

## Its most-cited devices
- K111512: Bonebac T-Plif Intervertebral Body Fusion Device System (2011), cited by 1

## Recent decisions
- K111512: Bonebac T-Plif Intervertebral Body Fusion Device System (Oct 26, 2011)

Source page: https://510kreport.com/company/thompson-mis