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Sign in to claim this brandBioplate, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 570 S. Melrose St., Placentia, CA, 92870
- Website
- bioplate.com
- —
- —
- [email protected]
- Phone
- 888-246-7528
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000518793
- DUNS Number
- 838734093
Catalogue (1156)
Page 2 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | SCR8-05-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3586[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3148 | FDA UDI | Class II | Active |
| Bioplate® | 81-2024-CP | FDA UDI | Class I | Active |
| Bioplate® | P1MC-36-43[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T4L5H1 | FDA UDI | Class II | Active |
| Bioplate® | P4LR-04-24[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3594 | FDA UDI | Class II | Unknown |
| CranioFit | KT-T7L15H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-5890 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-15-05 | FDA UDI | Class II | Active |
| Bioplate® | P8HP-07-16 | FDA UDI | Class II | Active |
| CranioFit | KT-T5L16H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3379[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR8-03-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L12H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-2078 | FDA UDI | Class II | Active |
| Bioplate® | P2NW-06-17 | FDA UDI | Class II | Active |
| Bioplate® | CAS2-01 | FDA UDI | Class I | Active |
| Bioplate® | 81-2016 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-04-01 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-15-01 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-05-05 | FDA UDI | Class II | Active |
| Bioplate® | P2CW-06-27 | FDA UDI | Class II | Active |
| Bioplate® | 81-2022 | FDA UDI | Class I | Active |
| Bioplate® | 81-3490 | FDA UDI | Class I | Active |
| CranioFit | KT-T6L6H1 | FDA UDI | Class II | Active |
| Bioplate® | ASB2-40 | FDA UDI | Class I | Active |
| Bioplate® | 81-3415 | FDA UDI | Class I | Active |
| CranioFit | KT-T2L4H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-17-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3372 | FDA UDI | Class II | Active |
| Bioplate® | 81-3140-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5745-CP | FDA UDI | Class II | Active |
| Bioplate® | P3BX-04-11 | FDA UDI | Class II | Active |
| CranioFit | KT-T3L16H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3342 | FDA UDI | Class I | Active |
| Bioplate® | 81-3180 | FDA UDI | Class II | Active |
| Bioplate® | 81-3126 | FDA UDI | Class I | Active |
| Bioplate® | 81-2019 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-17-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P8BN-06-16[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3143 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L11H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-5742 | FDA UDI | Class II | Active |
| Bioplate® | 81-3359 | FDA UDI | Class II | Active |
| Bioplate® | 81-3360 | FDA UDI | Class I | Active |
| CranioFit | KT-T3L17H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T9L1H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-11-05[US] | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (2)
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 |
|---|---|---|---|---|
| Mar 31, 2010 | Z-0143-2012 | — | terminated | There is potential defect in seal of the sterile barrier containing the device. |
| Sep 12, 2006 | Z-0043-2007 | — | terminated | Lack of device sterilization: An internal investigation found products were released for distribution labeled as sterile, but the lot was not sterilized. |