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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 7 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | SCD3-05-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T5L3H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3161-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5888 | FDA UDI | Class II | Active |
| Bioplate® | 81-1042 | FDA UDI | Class II | Active |
| Bioplate® | P2XB-06-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-7461 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-15-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3105 | FDA UDI | Class I | Active |
| Bioplate® | SCR2-08-50 | FDA UDI | Class II | Active |
| Bioplate® | P2SW-08-31 | FDA UDI | Class II | Active |
| Bioplate® | P2CW-04-19 | FDA UDI | Class II | Active |
| Bioplate® | 81-3039 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-03-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-2009 | FDA UDI | Class II | Active |
| Bioplate® | 81-3144[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T3L12H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-1044 | FDA UDI | Class II | Active |
| Bioplate® | 81-3573[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2014 | FDA UDI | Class II | Active |
| Bioplate® | 81-2021 | FDA UDI | Class I | Active |
| Bioplate® | 81-5771 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L3H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3038[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE4-04-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3519 | FDA UDI | Class II | Active |
| Bioplate® | 81-3025-CP | FDA UDI | Class II | Active |
| Bioplate® | P2SB-04-19 | FDA UDI | Class II | Active |
| Bioplate® | 81-3026[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2077 | FDA UDI | Class II | Active |
| Bioplate® | 81-3065 | FDA UDI | Class I | Active |
| Bioplate® | 81-3146 | FDA UDI | Class II | Active |
| Bioplate® | 81-3119 | FDA UDI | Class I | Active |
| Bioplate® | SCR8-06-05 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L16H2 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-05-50 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-06-01 | FDA UDI | Class II | Active |
| Bioplate® | P2BW-08-24 | FDA UDI | Class II | Active |
| Bioplate® | 81-2007-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-2075 | FDA UDI | Class II | Active |
| Bioplate® | 81-3355 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-08-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3141 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L17H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3103 | FDA UDI | Class I | Active |
| Bioplate® | 81-7366 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-03-50[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR8-05-01 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-03-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-7460 | FDA UDI | Class I | 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. |