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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 10 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tissue-Tek® SmartWrite® | 9045 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4156-02 | FDA UDI | Class I | Active |
| Genemed® | 60-0074-7 | FDA UDI | Class I | Active |
| Tissue-Tek® Genie® | 8408-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8319-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8356-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8268-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4183 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8867-G004 | FDA UDI | Class I | Active |
| Genemed® | 61-0093 | FDA UDI | Class I | Active |
| Genemed® | 61-0187 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8304-M250 | FDA UDI | Class I | Active |
| Genemed® | 61-0077 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8283-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4135-01 | FDA UDI | Class I | Active |
| Genemed® | 61-0058 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8535-C010 | EUDAMEDFDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4793 | FDA UDI | Class I | Active |
| Histo-Tek® | 9347 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 8172 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8352-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4223 | FDA UDI | Class I | Active |
| Tissue-Tek® Genie® | 8481-M100 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8129 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8398-C010 | FDA UDI | Class I | Active |
| Genemed® | 60-0138-7 | FDA UDI | Class I | Active |
| Tissue-Tek® SCA™ | 4772 | FDA UDI | Class I | Active |
| Tissue-Tek Xpress® x120 | 7730 | FDA UDI | Class I | Active |
| Genemed® | 60-0039-7 | FDA UDI | Class I | Active |
| Accu-Edge® | 4685 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4117-02 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8269-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® PRO | 8836-K250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® DUO | 8486-C010 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8289-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Paraform® | 7039 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4179 | FDA UDI | Class I | Active |
| Genemed® | 60-0001-7 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8184 | FDA UDI | Class I | Active |
| Genemed® | 52-0022 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4117-01 | FDA UDI | Class I | Active |
| Tissue-Tek® | 4456 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8500-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8270-M250 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8271-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® | 8183 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8225-M250 | FDA UDI | Class I | Active |
| Tissue-Tek® Uni-Cassette® | 4118-02 | FDA UDI | Class I | Active |
| Tissue-Tek Genie® | 8331-C010 | FDA UDI | Class I | Active |
| Tissue-Tek® Accu-Edge® | 4683 | 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. |