# Magnolia Medical Technologies

- Location (FDA's records): Seattle, WA
- FDA decisions: 4 (2020–2025): 4 510(k) clearances
- Names in FDA's records: Magnolia Medical Technologies (2); Magnolia Medical Technologies, Inc. (2)
- Product codes: JKA (3), FPA (1)
- 510(k) review time since 2016: median 157 days, against 173 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 5 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bd Vacutainer Systems Preanalyical Solutions: 1 (https://510kreport.com/company/bd-vacutainer-systems-preanalyical-solutions)

## Firms that cite its devices most
- Lifeoutcomes, LLC: 1 (https://510kreport.com/company/lifeoutcomes)
- Kurin, Inc.: 1 (https://510kreport.com/company/kurin)
- Velano Vascular: 1 (https://510kreport.com/company/velano-vascular)

## Its most-cited devices
- K192247: Steripath Gen2 Blood Collection System (2020), cited by 3
- K200661: Steripath Micro Blood Collection System (2020), cited by 2

## Recent decisions
- K251812: Steripath® Flow™ Blood Collection System (Sep 25, 2025)
- K222299: Steripath Micro Blood Collection System (Nov 30, 2022)
- K200661: Steripath Micro Blood Collection System (Oct 8, 2020)
- K192247: Steripath Gen2 Blood Collection System (Feb 28, 2020)

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