Is this your brand? Sign in to claim ownership.
Sign in to claim this brandMAGNOLIA MEDICAL TECHNOLOGIES, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 220 W Mercer St., Seattle, WA, 98119
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3009976527
- DUNS Number
- —
Catalogue (44)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SteriPath Gen2, 21G | 2700-21-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4005-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4000-23UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4010-23UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4000-UN-EN | FDA UDI | Class II | Active |
| Steripath Micro | 40BD-23UT-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 21G, 10ml | 2710-21-EN | FDA UDI | Class II | Active |
| Steripath | 2710-23UT-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 21G, BD | 27BD-21-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 21G, 20ml | 2720-21-EN | FDA UDI | Class II | Active |
| Steripath | 2720-21UT-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 23G, BD | 27BD-23-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4005-23UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4020-21UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4010-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4005-UN-EN | FDA UDI | Class II | Active |
| Steripath | 2700-23UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4010-21UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4005-21UT-EN | FDA UDI | Class II | Active |
| Steripath | 2710-21UT-EN | FDA UDI | Class II | Active |
| Steripath | 27BD-23UT-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, Luer | 2700-EN | FDA UDI | Class II | Active |
| Steripath | 2700-21UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4000-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4010-UN-EN | FDA UDI | Class II | Active |
| Steripath Micro | 40BD-21UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4000-21UT-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, Luer, BD | 27BD-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, Luer, 20ml | 2720-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4020-EN | FDA UDI | Class II | Active |
| Steripath Micro | 40BD-UN-EN | FDA UDI | Class II | Active |
| Steripath | 27BD-21UT-EN | FDA UDI | Class II | Active |
| Steripath Micro | 40BD-EN | FDA UDI | Class II | Active |
| Steripath Micro | 4020-UN-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 23G, 10ml | 2710-23-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, Luer, TS | 27TS-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 23G, TS | 27TS-23-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 21G, TS | 27TS-21-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, 23G | 2700-23-EN | FDA UDI | Class II | Active |
| SteriPath Gen2, Luer, 10ml | 2710-EN | FDA UDI | Class II | Active |
| Steripath Micro Blood Collection System | K222299 | FDA 510(k) | Class II | Active |
| Steripath Micro Blood Collection System | K200661 | FDA 510(k) | Class II | Active |
| Steripath Gen2 Blood Collection System | K192247 | FDA 510(k) | Class II | Active |
| Steripath® Flow™ Blood Collection System | K251812 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 2, 2021 | Z-0318-2022 | — | terminated | Due to an uptick of complaints associated with premature needle retraction of blood collection system. |
| Aug 2, 2021 | Z-2393-2021 | — | terminated | Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU). |