# VPIX Medical, Inc.

- Location (FDA's records): Daejeon, KR
- FDA decisions: 4 (2024–2026): 4 510(k) clearances
- Product codes: GWG (2), OWN (1), QFX (1)
- 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
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Mauna Kea Technologies: 1 (https://510kreport.com/company/mauna-kea-technologies)

## Recent decisions
- K260315: cCeLL - In vivo (Oct 16, 2026)
- K254030: cCeLL405 (Oct 2, 2026)
- K251852: cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200) (Feb 13, 2026)
- K233391: cCeLL - In vivo (Aug 21, 2024)

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