# Venowave, Inc.

- Location (FDA's records): Stouffville, Ontario, CA
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: JOW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Medical Compression Systems (Dbn), Ltd.: 1 (https://510kreport.com/company/medical-compression-systems-dbn)

## Firms that cite its devices most
- Thermabright: 1 (https://510kreport.com/company/thermabright)
- Dimedi Co., Ltd.: 1 (https://510kreport.com/company/dimedi)

## Its most-cited devices
- K073028: Venowave Models VW5-6, VW5-10, VW5-20 and VW5-30 (2008), cited by 2

## Recent decisions
- K073028: Venowave Models VW5-6, VW5-10, VW5-20 and VW5-30 (Mar 7, 2008)

Source page: https://510kreport.com/company/venowave