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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 (923)
Page 11 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek® Paraform® | 7024 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8334-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® | 4010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8234-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7167 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8363-C010 | FDA UDI | Class I | Unknown |
| Tissue-Tek® Paraform® | 7022 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4451 | FDA UDI | Class I | Active |
| Histo-Tek® | 9343 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8252-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® | 6508 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8088 | FDA UDI | Class I | Active |
| Histo-Tek® | 9221 | FDA UDI | Class I | Active |
| Histo-Tek® | 9357 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8179 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® PRO | 8866-G004 | FDA UDI | Class I | Active |
| Genemed® | 61-0001 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8271-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8615-G001 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® | 5989 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7045 | FDA UDI | Class I | Active |
| Genemed® | 61-0019 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8372-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8267-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8500-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8157 | FDA UDI | Class I | Active |
| Genemed® | 61-0085 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8326-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9022 | FDA UDI | Class I | Active |
| Genemed® | 10-0037 | FDA UDI | Class I | Active |
| Genemed® | 60-0187-7 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8187 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8325-C010 | EUDAMEDFDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7187 | EUDAMEDFDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8538-C010 | EUDAMEDFDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8342-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8282-M250 | FDA UDI | Class I | Active |
| Histo-Tek® | 9348 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8255-C010 | FDA UDI | Class I | Active |
| Genemed® | 61-0020 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8334-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8256-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8086 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8473-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8325-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8326-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Glas™ | 6419 | FDA UDI | Class I | Active |
| Genemed® | 52-0023 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® | 5991 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4120-01 | 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. |