# Promex Technologies, LLC

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: KNW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Promex, Inc.: 1 (https://510kreport.com/company/promex)
- Vibronics: 1 (https://510kreport.com/company/vibronics)

## Firms that cite its devices most
- Pfm Medical, Inc.: 1 (https://510kreport.com/company/pfm-medical)

## Its most-cited devices
- K111765: Full Core Biopsy System (2011), cited by 1

## Recent decisions
- K111765: Full Core Biopsy System (Sep 6, 2011)

Source page: https://510kreport.com/company/promex-technologies