# Compass Intl., Inc.

- Location (FDA's records): Rochester, MN
- FDA decisions: 2 (1995–1997): 2 510(k) clearances
- Product codes: HAW (2)
- Predicates its devices cite: 3 (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
- Stereotactic Medical Systems, Inc.: 1 (https://510kreport.com/company/stereotactic-medical-systems)
- I.S.G. Technologies, Inc.: 1 (https://510kreport.com/company/isg-technologies)

## Firms that cite its devices most
- Fiagon GmbH: 1 (https://510kreport.com/company/fiagon)
- Orthosoft, Inc.: 1 (https://510kreport.com/company/orthosoft)
- Ultraguide, Ltd.: 1 (https://510kreport.com/company/ultraguide)

## Its most-cited devices
- K935456: Regulus Measurement Unit (1995), cited by 2
- K964229: Regulus Navigator (1997), cited by 2

## Recent decisions
- K964229: Regulus Navigator (Aug 19, 1997)
- K935456: Regulus Measurement Unit (Oct 13, 1995)

Source page: https://510kreport.com/company/compass-intl