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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 10 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | CRSH-12 | FDA UDI | Class I | Active |
| Bioplate® | P2CK-04-22 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-11-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T1L7H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3588[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3067 | FDA UDI | Class I | Active |
| CranioFit | KT-T6L18H1 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-05-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3371 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-08-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3054 | FDA UDI | Class II | Active |
| Bioplate® | P4ST-06-36 | FDA UDI | Class II | Active |
| Bioplate® | 81-2080 | FDA UDI | Class II | Active |
| Bioplate® | 81-5785 | FDA UDI | Class II | Active |
| Bioplate® | 81-5723[US] | FDA UDI | Class II | Active |
| Bioplate® | P2TW-04-17 | FDA UDI | Class II | Active |
| Bioplate® | ASB4-45 | FDA UDI | Class I | Active |
| Bioplate® | DBP4-20 | FDA UDI | Class I | Active |
| Bioplate® | P2ZL-04-16 | FDA UDI | Class II | Active |
| CranioFit | KT-T3L5H1 | FDA UDI | Class II | Active |
| Bioplate® | P8BN-06-16 | FDA UDI | Class II | Active |
| Bioplate® | P8HP-11-18 | FDA UDI | Class II | Active |
| Bioplate® | 81-3052 | FDA UDI | Class II | Active |
| Bioplate® | P4LR-08-40 | FDA UDI | Class II | Active |
| Bioplate® | 81-7320 | FDA UDI | Class II | Active |
| CranioFit | KT-T9L7H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-04-01 | FDA UDI | Class II | Active |
| Bioplate® | P4ST-04-24[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE8-03-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3417 | FDA UDI | Class I | Active |
| Bioplate® | SCR2-10-50 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L3H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3059 | FDA UDI | Class II | Active |
| Bioplate® | 81-3164 | FDA UDI | Class II | Active |
| Bioplate® | 81-4209 | FDA UDI | Class I | Active |
| Bioplate® | 81-3426 | FDA UDI | Class I | Active |
| Bioplate® | 81-5728[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5734-CP | FDA UDI | Class II | Active |
| Bioplate® | SCD2-04-05 | FDA UDI | Class II | Active |
| Bioplate® | P8BX-04-09 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-05-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P2LW-04-13 | FDA UDI | Class II | Active |
| Bioplate® | 81-2073 | FDA UDI | Class II | Active |
| Bioplate® | 81-2006 | FDA UDI | Class II | Active |
| Bioplate® | ASB4-40 | FDA UDI | Class I | Active |
| CranioFit | KT-T8L3H1 | FDA UDI | Class II | Active |
| Bioplate® | P2RW-04-15 | FDA UDI | Class II | Active |
| Bioplate® | 81-7368 | FDA UDI | Class II | Active |
| Bioplate® | P2TB-04-20 | FDA UDI | Class II | Active |
| CranioFit | KT-T8L10H2 | 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. |