# Pdo Max, Inc.

- Location (FDA's records): Liverpool, NY
- FDA decisions: 2 (2019–2021): 2 510(k) clearances
- Product codes: NEW (2)
- Predicates its devices cite: 2 (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
- Feeltech Co., Ltd.: 1 (https://510kreport.com/company/feeltech)
- Angiotech: 1 (https://510kreport.com/company/angiotech)

## Recent decisions
- K210871: PDO Max Suture with Dual Needle (Dec 17, 2021)
- K190245: PDS Barbed Suture, PDO MAXX Threads (Jun 4, 2019)

Source page: https://510kreport.com/company/pdo-max