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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 20 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | DBP2-10 | FDA UDI | Class I | Active |
| Bioplate® | 81-2037[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5729[US] | FDA UDI | Class II | Active |
| Bioplate® | P4SB-04-30 | FDA UDI | Class II | Active |
| Bioplate® | 81-3145 | FDA UDI | Class II | Active |
| Bioplate® | P2RP-17-34[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3044 | FDA UDI | Class I | Active |
| Bioplate® | P2CB-06-27 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L16H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-5722[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3068 | FDA UDI | Class I | Active |
| Bioplate® | 81-4206 | FDA UDI | Class I | Active |
| Bioplate® | 81-3303 | FDA UDI | Class II | Active |
| Bioplate® | P2CP-08-30 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L9H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-5891 | FDA UDI | Class II | Active |
| Bioplate® | P2RP-17-34 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-06-05 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L13H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3356 | FDA UDI | Class II | Active |
| Bioplate® | P2SB-04-21 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-05-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3050 | FDA UDI | Class II | Active |
| Bioplate® | P2MC-33-48 | FDA UDI | Class II | Active |
| Bioplate® | P4SK-06-41 | FDA UDI | Class II | Active |
| Bioplate® | 81-3047 | FDA UDI | Class I | Active |
| Bioplate® | ASHB-44 | FDA UDI | Class I | Active |
| Bioplate® | 81-2001 | FDA UDI | Class II | Active |
| Bioplate® | 81-2025 | FDA UDI | Class I | Active |
| Bioplate® | 81-5744-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-2047 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-10-05[US] | FDA UDI | Class II | Active |
| Bioplate® | ASHB-45 | FDA UDI | Class I | Active |
| CranioFit | KT-T8L7H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-5895 | FDA UDI | Class II | Active |
| Bioplate® | P4ST-16-99[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3101 | FDA UDI | Class I | Active |
| Bioplate® | 81-5885 | FDA UDI | Class II | Active |
| Bioplate® | P8ST-16-62[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2000[US] | FDA UDI | Class II | Active |
| Bioplate® | SCP2-12-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-10-05 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-12-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-2065-CP | FDA UDI | Class II | Active |
| Bioplate® | P8YP-06-17 | FDA UDI | Class II | Active |
| Bioplate® | P2SK-02-14-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-7311 | FDA UDI | Class II | Active |
| Bioplate® | 81-3075 | FDA UDI | Class I | Active |
| CranioFit | KT-T4L14H2 | FDA UDI | Class II | Active |
| Bioplate® | P8ST-06-22[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. |