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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 4 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | SCE2-10-01 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-14-01[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR8-08-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3040 | FDA UDI | Class II | Active |
| Bioplate® | ASB2-40-SALE | FDA UDI | Class I | Active |
| Bioplate® | 81-3131 | FDA UDI | Class II | Active |
| Bioplate® | 81-3301 | FDA UDI | Class II | Active |
| Bioplate® | 81-3021[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2034 | FDA UDI | Class I | Active |
| Bioplate® | 81-2004[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T4L8H2 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-11-05 | FDA UDI | Class II | Active |
| CranioFit | KT-T8L6H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-2073[US] | FDA UDI | Class II | Active |
| Bioplate® | DBP2-04 | FDA UDI | Class I | Active |
| Bioplate® | 81-3028-CP | FDA UDI | Class II | Active |
| Bioplate® | P3ST-16-86 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-05-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-5750 | FDA UDI | Class I | Active |
| Bioplate® | 81-3521 | FDA UDI | Class II | Active |
| Bioplate® | 81-3367 | FDA UDI | Class I | Active |
| CranioFit | KT-T4L16H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L4H1 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L4H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3048-CP | FDA UDI | Class II | Active |
| CranioFit | KT-T6L12H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-2067[US] | FDA UDI | Class II | Active |
| Bioplate® | ASB2-20-SALE | FDA UDI | Class I | Active |
| Bioplate® | 81-3574 | FDA UDI | Class II | Active |
| Bioplate® | P2SK-02-14 | FDA UDI | Class II | Active |
| Bioplate® | 81-3491 | FDA UDI | Class I | Active |
| Bioplate® | 81-3516 | FDA UDI | Class II | Unknown |
| Bioplate® | SCR4-04-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-5730[US] | FDA UDI | Class II | Active |
| Bioplate® | P2XW-06-13 | FDA UDI | Class II | Active |
| Bioplate® | P2XP-06-13 | FDA UDI | Class II | Active |
| Bioplate® | ASB8-25 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-05-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3304 | FDA UDI | Class II | Active |
| Bioplate® | 81-5898 | FDA UDI | Class II | Active |
| Bioplate® | 81-3132 | FDA UDI | Class II | Active |
| Bioplate® | 81-5751 | FDA UDI | Class I | Active |
| Bioplate® | P4XP-06-20 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-03-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3023 | FDA UDI | Class II | Active |
| Bioplate® | 81-3358[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T9L5H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3140 | FDA UDI | Class II | Active |
| Bioplate® | P2CB-04-19 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-03-01 | 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. |