# Coombs Medical Device Consulting

- Location (FDA's records): Alameda, CA
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: DRE (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Maxxim Medical: 1 (https://510kreport.com/company/maxxim-medical)

## Firms that cite its devices most
- Avalon Laboratories, LLC: 1 (https://510kreport.com/company/avalon-laboratories)
- Lifetech Scientific (Shenzhen) Co., Ltd.: 1 (https://510kreport.com/company/lifetech-scientific-shenzhen)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Endoscopic Technologies, Inc. D/B/A Estech: 1 (https://510kreport.com/company/endoscopic-technologies-d-b-a-estech)

## Its most-cited devices
- K070749: Estech Percutaneous Insertion Dilator Kit (2007), cited by 4

## Recent decisions
- K070749: Estech Percutaneous Insertion Dilator Kit (Oct 24, 2007)

Source page: https://510kreport.com/company/coombs-medical-device-consulting