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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 (921)
Page 1 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek Genie® | 8381-C010 | FDA UDI | Class I | Active |
| Genemed® | 70-0028-15 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8241-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7184 | FDA UDI | Class I | Active |
| Genemed® | 61-0017 | FDA UDI | Class I | Active |
| Histo-Tek® | 9345 | FDA UDI | Class I | Active |
| Histo-Tek® | 9341 | FDA UDI | Class I | Active |
| Genemed® | 61-0006 | FDA UDI | Class I | Active |
| Genemed® | 61-0090 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8501-M250 | FDA UDI | Class I | Active |
| Genemed® | 10-0046 | FDA UDI | Class I | Active |
| Tissue-Tek® Feather® | 7089 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8281-M250 | FDA UDI | Class I | Active |
| Accu-Cut® SRM™ 200 | 1429N | FDA UDI | Class I | Active |
| Histo-Tek® | 9340 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4087 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8340-M250 | FDA UDI | Class I | Active |
| Histo-Tek® SL | 1900 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4164 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8487-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8324-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8382-M250 | FDA UDI | Class I | Active |
| Genemed® | 10-0001 | FDA UDI | Class I | Active |
| Histo-Tek® | 9342 | FDA UDI | Class I | Active |
| Tissue-Tek® Quick-Ray™ | 8010 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7078 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7049 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7165 | FDA UDI | Class I | Active |
| Genemed® | 61-0125 | FDA UDI | Class I | Active |
| Tissue-Tek Xpress® | 7750 | FDA UDI | Class I | Active |
| Tissue-Tek® | 6021 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4121 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9023 | FDA UDI | Class I | Active |
| Histo-Tek® | 9344 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8622-G006 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8407-C010 | FDA UDI | Class I | Active |
| Genemed® | 60-0092-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8308-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8170 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8300-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8469-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Feather® | 4980 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9021 | FDA UDI | Class I | Active |
| Tissue-Tek® Cryomold® | 4557 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7052 | FDA UDI | Class I | Active |
| Genemed® | 61-0158 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8336-C010 | FDA UDI | Class I | Active |
| Histo-Tek® | 9229 | FDA UDI | Class I | Active |
| Histo-Tek® | 9358 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8242-M250 | 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. |