# MicroVention, Inc., d/b/a Terumo Neuro

- Location (FDA's records): Aliso Viejo, CA
- FDA decisions: 3 (2026–2026): 3 510(k) clearances
- Names in FDA's records: MicroVention, Inc., d/b/a Terumo Neuro (2); Microvention Inc. d/b/a Terumo Neuro (1)
- Product codes: QJP (2), QEZ (1)
- 510(k) review time since 2016: median 29 days, against 141 for FDA's reviews in the same codes and years (2 of 3 faster)
- 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
- MicroVention, Inc.: 2 (https://510kreport.com/company/microvention)
- Inari Medical, Inc.: 1 (https://510kreport.com/company/inari-medical)

## Recent decisions
- K254035: Mayumi™ Thrombectomy System (Sep 3, 2026)
- K261808: ISAAC Neurovascular Navigation Catheter (Jun 30, 2026)
- K261549: BOBBY Balloon Guide Catheter (Jun 9, 2026)

Source page: https://510kreport.com/company/microvention-d-b-a-terumo-neuro