# Watermark Medical

- Location (FDA's records): Brookfield, WI
- FDA decisions: 4 (2012–2017): 4 510(k) clearances
- Names in FDA's records: Watermark Medical (3); Watermark Medical, Inc. (1)
- Product codes: DRG (2), DXN (1), MNR (1)
- Predicates its devices cite: 4 (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
- Honeywell Hommed, LLC: 3 (https://510kreport.com/company/honeywell-hommed)
- Advanced Brain Monitoring, Inc.: 1 (https://510kreport.com/company/advanced-brain-monitoring)

## Firms that cite its devices most
- Andon Health Co, Ltd.: 1 (https://510kreport.com/company/andon-health)

## Its most-cited devices
- K120320: Connected Care Clinical Application (2012), cited by 1

## Recent decisions
- K160499: Apnea Risk Evaluation System (ARES), Model 620 (Apr 24, 2017)
- K120320: Connected Care Clinical Application (Aug 14, 2012)
- K120325: Connected Care Mobile Application (Jul 18, 2012)
- K120470: MIPAL (Jun 8, 2012)

Source page: https://510kreport.com/company/watermark-medical