# Artventive Medical Group, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 3 (2014–2022): 3 510(k) clearances
- Product codes: KRD (3)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (2 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
- Aga Medical Corp.: 2 (https://510kreport.com/company/aga-medical)
- Reverse Medical Corporation: 1 (https://510kreport.com/company/reverse-medical)

## Its most-cited devices
- K150402: Endoluminal Occlusion System-EOS (2015), cited by 1
- K133924: Endoluminal Occlusion System (Eos) (2014), cited by 1

## Recent decisions
- K212057: Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS (Mar 1, 2022)
- K150402: Endoluminal Occlusion System-EOS (Sep 25, 2015)
- K133924: Endoluminal Occlusion System (Eos) (Dec 3, 2014)

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