# Poiesis Medical, LLC

- Location (FDA's records): Jupiter, FL
- FDA decisions: 1 (2018–2018): 1 510(k) clearance
- Product codes: EZL (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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 Technology Development Corp.: 1 (https://510kreport.com/company/medical-technology-development)

## Recent decisions
- K173533: Duette 100% Silicone Dual-Balloon, Temperature-Sensing Catheter (Mar 29, 2018)

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