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Sign in to claim this brandSakura Finetek USA, Inc
United States·US-MF-000022208
Last updated June 8, 2026
Information
- Country
- United States
- Address
- 1750, West 214th Street, Torrance, CA, United States
- Website
- sakuraus.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Solmaz Shaida
- EUDAMED SRN
- US-MF-000022208
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (924)
Page 12 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek® Uni-Cassette® | 4120-01 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® Ultra™ II | 3982 | FDA UDI | Class I | Active |
| Genemed® | 61-0190 | FDA UDI | Class I | Active |
| Tissue-Tek® TEC™ 6 | 5250 | FDA UDI | Class I | Active |
| VisionTek® | 9000 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7079 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4770 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8314-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8462-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8267-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8350-M250 | FDA UDI | Class I | Active |
| Genemed® | 61-0192 | FDA UDI | Class I | Active |
| Tissue-Tek Prisma® | 6190 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7037 | FDA UDI | Class I | Active |
| Genemed® | 61-0062 | FDA UDI | Class I | Active |
| Genemed® | 60-0209-15 | FDA UDI | Class I | Active |
| Genemed® | 60-0219-15 | FDA UDI | Class I | Active |
| Genemed® | 61-0013 | FDA UDI | Class I | Active |
| Tissue-Tek® Glas™ g2 | 6500 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8249-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® CISH | 9809-G006 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9020 | FDA UDI | Class I | Active |
| Genemed® | 10-0034 | FDA UDI | Class I | Active |
| Genemed® | 60-0012-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® | 4038 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8320-M250 | FDA UDI | Class I | Active |
| Genemed® | 61-0142 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8865-G001 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9052 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8309-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8333-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Xpress® | 7110 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8286-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8600-K040 | FDA UDI | Class I | Active |
| Histo-Tek® | 9234 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8238-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8335-C010 | FDA UDI | Class I | Unknown |
| Tissue-Tek Genie® | 8303-C010 | EUDAMEDFDA UDI | Class I | Active |
| Histo-Tek® | 9350 | FDA UDI | Class I | Active |
| Genemed® | 60-0181-7 | FDA UDI | Class I | Active |
| Genemed® | 60-0011-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8521-C010 | EUDAMEDFDA UDI | Class I | Active |
| Histo-Tek® | 4220 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8300-M250 | FDA UDI | Class I | Active |
| Histo-Tek® | 9235 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8223-C010 | FDA UDI | Class I | Active |
| Genemed® | 10-0032 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8535-M250 | FDA UDI | Class I | Active |
| Genemed® | 10-0033 | FDA UDI | Class I | Active |
| Cyto-Tek® 2500 | 4301 | FDA UDI | Class I | Active |
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FDA Recalls (1)
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 |
|---|---|---|---|---|
| Apr 16, 2014 | Z-1748-2014 | — | terminated | This Lot has variations in melting temperature. |