# Kurin, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 3 (2019–2023): 3 510(k) clearances
- Product codes: JKA (3)
- 510(k) review time since 2016: median 210 days, against 181 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (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
- Pathway, LLC: 2 (https://510kreport.com/company/pathway)
- Nexus Medical, LLC: 1 (https://510kreport.com/company/nexus-medical)
- Magnolia Medical Technologies: 1 (https://510kreport.com/company/magnolia-medical-technologies)

## Recent decisions
- K220677: Kurin Blood Culture Collection Set with Kurin Lock Technology (Apr 28, 2023)
- K191832: Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models M-21221, M-21223, D-21221, D-21223, T-21221, T-21223) (Feb 4, 2020)
- K181895: Kurin PIV Blood Collection Set with High Pressure (Jan 18, 2019)

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