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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 13 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Genemed® | 60-0038-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8539-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8295-C010 | FDA UDI | Class I | Active |
| Histo-Tek® | 9225 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4045 | FDA UDI | Class I | Active |
| Tissue-Tek Film® | 4740 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8742-G001 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7183 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8292-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0077-7 | FDA UDI | Class I | Active |
| Tissue-Tek VIP® | 4005 | FDA UDI | Class I | Active |
| Genemed® | 61-0050 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4162 | FDA UDI | Class I | Active |
| Tissue-Tek® | 5988 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8536-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Cryo3® | 5807 | EUDAMEDFDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8087 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7035 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8312-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8223-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4187 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8339-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8341-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0190-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8310-C010 | FDA UDI | Class I | Active |
| Genemed® | 10-0056 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9024 | FDA UDI | Class I | Active |
| Genemed® | 60-0060-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8447-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Mega-Cassette® | 4166 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8503-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8487-M100 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8295-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8637-K001 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9031 | FDA UDI | Class I | Active |
| Tissue-Tek® NanoMold™ | 4216 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8327-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4125 | FDA UDI | Class I | Active |
| Tissue-Tek® TEC™ 6 | 5782 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8310-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8636-K001 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8260-C010 | FDA UDI | Class I | Active |
| Genemed® | 60-0010-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7073 | FDA UDI | Class I | Active |
| Genemed® | 54-0003 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4114 | FDA UDI | Class I | Active |
| Genemed® | 61-0118 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8290-M250 | FDA UDI | Class I | Unknown |
| Tissue-Tek® Uni-Cassette® | 8135 | FDA UDI | Class I | Active |
| Histo-Tek® | 9354 | 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. |