# Retropsoas Technologies, LLC

- Location (FDA's records): Frontenac, MO
- FDA decisions: 2 (2024–2024): 2 510(k) clearances
- Product codes: ETN (1), MAX (1)
- Predicates its devices cite: 3 (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
- Nvision Biomedical Technologies, Inc.: 3 (https://510kreport.com/company/nvision-biomedical-technologies)

## Recent decisions
- K242457: EARP Interbody System (Oct 7, 2024)
- K241917: EARP Nerve Cuff Electrode (Jul 31, 2024)

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