# Leadoptik, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 2 (2025–2025): 2 510(k) clearances
- Product codes: NQQ (1), KTI (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
- Ninepoint Medical, Inc.: 1 (https://510kreport.com/company/ninepoint-medical)
- Olympus Surgical Technologies America: 1 (https://510kreport.com/company/olympus-surgical-technologies-america)

## Recent decisions
- K251730: LIA Console  (542-7) (Dec 19, 2025)
- K251402: LIA-1 Catheter (542-1) (Dec 19, 2025)

Source page: https://510kreport.com/company/leadoptik