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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 18 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Genemed® | 10-0005 | FDA UDI | Class I | Active |
| Genemed® | 60-0065-7 | FDA UDI | Class I | Active |
| Genemed® | 60-0223-15 | FDA UDI | Class I | Active |
| Genemed® | 60-0113-7 | FDA UDI | Class I | Active |
| Genemed® | 61-0181 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9046 | FDA UDI | Class I | Active |
| Cyto-Tek® | 4310 | FDA UDI | Class I | Active |
| Genemed® | 10-0040 | FDA UDI | Class I | Active |
| Genemed® | 61-0008 | FDA UDI | Class I | Active |
| Histo-Tek® | 9238 | FDA UDI | Class I | Active |
| Histo-Tek® | 9228 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7075 | FDA UDI | Class I | Active |
| Genemed® | 60-0037-7 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® | 5992 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8117 | FDA UDI | Class I | Active |
| Genemed® | 10-0029 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8155 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8486-M100 | FDA UDI | Class I | Active |
| Genemed® | 61-0133-2 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® | 4012 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7188 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4170-02 | FDA UDI | Class I | Active |
| Genemed® | 60-0064-7 | FDA UDI | Class I | Active |
| Tissue-Tek AutoSection® | 5010 | FDA UDI | Class I | Active |
| VisionTek® | 9011 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7034 | FDA UDI | Class I | Active |
| Tissue-Tek Xpress® | 7109 | FDA UDI | Class I | Active |
| Tissue-Tek® Quick-Ray™ | 8018 | FDA UDI | Class I | Active |
| Genemed® | 61-0186 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4180-02 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9050 | FDA UDI | Class I | Active |
| Tissue-Tek® Quick-Ray™ | 8020 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7070 | FDA UDI | Class I | Active |
| Genemed® | 61-0174 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® Ultra™ II | 3980 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8484-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4118-01 | FDA UDI | Class I | Active |
| Genemed® | 61-0138 | FDA UDI | Class I | Active |
| Genemed® | 61-0064 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8485-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7040 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8180 | FDA UDI | Class I | Active |
| Histo-Tek® | 9356 | FDA UDI | Class I | Active |
| Tissue-Tek® NanoMold™ | 4219 | FDA UDI | Class I | Active |
| Genemed® | 60-0013-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4154-02 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8388-C010 | EUDAMED | Class C | Active |
| Tissue-Tek Genie® | 8276-M250 | EUDAMEDFDA UDI | Class C | Active |
| Tissue-Tek Genie® | 8386-C010 | EUDAMEDFDA UDI | Class C | Active |
| Tissue-Tek Genie® | 8280-M250 | EUDAMEDFDA UDI | Class C | 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. |