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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 5 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cryomold® | 4730 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8258-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4583 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8264-C010 | FDA UDI | Class I | Unknown |
| Tissue-Tek Genie® | 8224-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8521-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0022-7 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8182 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7019 | FDA UDI | Class I | Active |
| Genemed® | 61-0096 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8294-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8485-M100 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8394-M250 | FDA UDI | Class I | Active |
| Genemed® | 60-0193-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8304-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4171-01 | FDA UDI | Class I | Active |
| Genemed® | 61-0042 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8174 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7057 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8461-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8305-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8350-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Film® | 4740 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8333-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8482-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8301-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8317-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8226-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9030 | FDA UDI | Class I | Active |
| Accu-Cut® SRM™ 200 | 1441 | FDA UDI | Class I | Active |
| Genemed® | 60-0016-7 | FDA UDI | Class I | Active |
| Genemed® | 60-0017-7 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8285-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7046 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8243-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Lab Aid® Ultra™ II | 3990 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7041 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8279-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4194 | FDA UDI | Class I | Active |
| Genemed® | 52-0006 | FDA UDI | Class I | Active |
| Tissue-Tek® SmartWrite® | 9035 | FDA UDI | Class I | Active |
| Genemed® | 10-0020 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 9811-M100 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8473-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8519-C010 | FDA UDI | Class I | Active |
| Accu-Cut® SRM™ 200 | 1436 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4124 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4115 | FDA UDI | Class I | Active |
| Genemed® | 60-0066-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Cryo3® | 6201 | 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. |