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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 3 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek® Uni-Cassette® | 4119-01 | FDA UDI | Class I | Active |
| Tissue-Tek® TEC™ 6 | 5108 | FDA UDI | Class I | Active |
| Genemed® | 60-0170-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8253-C010 | FDA UDI | Class I | Active |
| Genemed® | 60-0002-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Glas™ g2 | 6417 | FDA UDI | Class I | Active |
| Tissue-Tek® Mega-Cassette | 4173 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7033 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4224 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4154-01 | FDA UDI | Class I | Active |
| Genemed® | 60-0118-7 | FDA UDI | Class I | Active |
| Tissue-Tek® NanoMold™ | 4215 | FDA UDI | Class I | Active |
| Genemed® | 60-0125-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8235-C010 | FDA UDI | Class I | Active |
| Genemed® | 61-0066 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4650 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8236-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4191 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8619-K100 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7015 | FDA UDI | Class I | Active |
| Genemed® | 10-0047 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® | 5990 | FDA UDI | Class I | Active |
| Histo-Tek® | 9224 | FDA UDI | Class I | Active |
| Genemed® | 60-0135-7 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4141 | FDA UDI | Class I | Active |
| Genemed® | 61-0054 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8302-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8232-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4786 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8307-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8336-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4797 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8317-M250 | FDA UDI | Class I | Active |
| Genemed® | 61-0011 | FDA UDI | Class I | Active |
| Genemed® | 60-0115-7 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4181 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8283-C010 | FDA UDI | Class I | Active |
| Genemed® | 54-0017 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8323-C010 | FDA UDI | Class I | Active |
| Genemed® | 10-0176 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8126 | FDA UDI | Class I | Active |
| Tissue-Tek Prisma® Plus | 6171 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8518-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4153-02 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® Ultra™ II | 3981 | FDA UDI | Class I | Active |
| Genemed® | 60-0019-7 | FDA UDI | Class I | Active |
| Genemed® | 61-0061 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8279-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0090-7 | FDA UDI | Class I | Active |
| Genemed® | 60-0192-7 | 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. |