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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 17 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek Genie® | 8257-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8394-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8618-G090 | FDA UDI | Class I | Active |
| Genemed® | 61-0184 | FDA UDI | Class I | Active |
| Genemed® | 60-0048-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8306-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4789 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4113 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4192 | FDA UDI | Class I | Active |
| Genemed® | 61-0014 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8244-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0078-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8383-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8224-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7076 | FDA UDI | Class I | Active |
| Genemed® | 10-0028 | FDA UDI | Class I | Active |
| Genemed® | 61-0028 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8339-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8316-M250 | FDA UDI | Class I | Active |
| Accu-Cut® SRM™ 300 LT | 1300 | FDA UDI | Class I | Active |
| Histo-Tek® | 1920 | FDA UDI | Class I | Active |
| Genemed® | 60-0050-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8045 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9048 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8234-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8372-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8090 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8381-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8384-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® | 4013 | FDA UDI | Class I | Active |
| Genemed® | 60-0186-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Cryo3® | 6209 | FDA UDI | Class I | Active |
| Tissue-Tek® Quick-Ray™ | 8019 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7032 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7047 | FDA UDI | Class I | Active |
| Histo-Tek® | 9227 | FDA UDI | Class I | Active |
| Tissue-Tek Xpress® | 7120 | FDA UDI | Class I | Active |
| Histo-Tek® | 9351 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® | 4011 | FDA UDI | Class I | Active |
| Tissue-Tek Prisma® | 6134 | FDA UDI | Class I | Active |
| Genemed® | 60-0018-7 | FDA UDI | Class I | Active |
| Genemed® | 61-0160 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® 6 | 6040 | FDA UDI | Class I | Active |
| Genemed® | 70-0027-15 | FDA UDI | Class I | Active |
| Genemed® | 60-0124-7 | FDA UDI | Class I | Active |
| Accu-Cut® SRM™ 200 | 1437 | FDA UDI | Class I | Active |
| Tissue-Tek® Cryo3® | 5809 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4171-02 | FDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4790 | FDA UDI | Class I | Active |
| Tissue-Tek® Quick-Ray™ | 8017 | 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. |