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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 9 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CranioFit | KT-T5L15H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-5729 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L5H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3018-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5712 | FDA UDI | Class II | Active |
| Bioplate® | ASB2-20 | FDA UDI | Class I | Active |
| Bioplate® | 81-5751-CP | FDA UDI | Class I | Active |
| CranioFit | KT-T9L16H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-2037 | FDA UDI | Class II | Active |
| Bioplate® | 81-3421 | FDA UDI | Class I | Active |
| Bioplate® | 81-2027-CP | FDA UDI | Class I | Active |
| Bioplate® | 81-2054-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-2002[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3380 | FDA UDI | Class I | Active |
| CranioFit | KT-T1L6H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-13-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3161 | FDA UDI | Class II | Active |
| Bioplate® | 81-2094 | FDA UDI | Class II | Active |
| Bioplate® | 81-3370 | FDA UDI | Class II | Active |
| Bioplate® | 81-3046 | FDA UDI | Class I | Active |
| Bioplate® | SCD8-04-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-5742[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-4209-CP | FDA UDI | Class I | Active |
| CranioFit | KT-T6L13H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3590 | FDA UDI | Class II | Active |
| CranioFit | KT-T3L7H1 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-05-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3018 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-08-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T8L14H2 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-04-50[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3528[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2012 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-05-05 | FDA UDI | Class II | Active |
| Bioplate® | P2SB-02-14[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR4-05-01 | FDA UDI | Class II | Active |
| Bioplate® | P4SB-06-43 | FDA UDI | Class II | Active |
| Bioplate® | P2HP-07-17 | FDA UDI | Class II | Active |
| CranioFit | KT-T4L11H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3483 | FDA UDI | Class I | Active |
| Bioplate® | 81-5725 | FDA UDI | Class II | Active |
| Bioplate® | 81-4205-CP | FDA UDI | Class I | Active |
| Bioplate® | 81-3135[US] | FDA UDI | Class II | Active |
| Bioplate® | DBP4-10 | FDA UDI | Class I | Active |
| CranioFit | KT-T1L18H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3018[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T8L8H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T1L2H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-2000 | FDA UDI | Class II | Active |
| Bioplate® | P2YB-05-18 | 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. |