# Compactcath, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 3 (2014–2018): 3 510(k) clearances
- Product codes: EZD (3)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- Coloplast Manufacturing Us, LLC: 1 (https://510kreport.com/company/coloplast-manufacturing-us)

## Its most-cited devices
- K140945: Compactcath Intermittent Urinary Catheter (2014), cited by 2
- K160858: CompactCath Intermittent Urinary Catheter (2016), cited by 1

## Recent decisions
- K180738: COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter (Jun 14, 2018)
- K160858: CompactCath Intermittent Urinary Catheter (Apr 26, 2016)
- K140945: Compactcath Intermittent Urinary Catheter (Aug 22, 2014)

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