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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 3 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CranioFit | KT-T8L15H2 | FDA UDI | Class II | Active |
| Bioplate® | P1MC-80-99 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-15-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3428 | FDA UDI | Class I | Active |
| Bioplate® | 81-3023-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3310 | FDA UDI | Class I | Active |
| Bioplate® | P4LL-04-24[US] | FDA UDI | Class II | Active |
| Bioplate® | P8CP-08-29[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3379 | FDA UDI | Class II | Active |
| Bioplate® | P8XP-07-16[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3416 | FDA UDI | Class I | Active |
| Bioplate® | P4YP-05-22[US] | FDA UDI | Class II | Active |
| Bioplate® | ABP2-10 | FDA UDI | Class I | Active |
| Bioplate® | 81-3043 | FDA UDI | Class II | Active |
| Bioplate® | 81-3050[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR4-09-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-2053[US] | FDA UDI | Class II | Active |
| Bioplate® | DBZ3-06 | FDA UDI | Class I | Active |
| Bioplate® | 81-3082 | FDA UDI | Class I | Active |
| Bioplate® | P2RW-05-21[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3013 | FDA UDI | Class II | Active |
| Bioplate® | P2CW-08-30 | FDA UDI | Class II | Active |
| Bioplate® | 81-2076 | FDA UDI | Class II | Active |
| Bioplate® | 81-2003[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE8-06-05[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T5L17H2 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-10-01 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-13-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L14H2 | FDA UDI | Class II | Active |
| Bioplate® | P4LL-04-20 | FDA UDI | Class II | Active |
| Bioplate® | DBP4-06-SALE | FDA UDI | Class I | Active |
| Bioplate® | SCE2-06-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P4LL-08-40[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3029-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5792 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-04-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-08-05[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T3L1H1 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L15H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3102 | FDA UDI | Class I | Active |
| Bioplate® | 81-2048 | FDA UDI | Class II | Active |
| Bioplate® | P4LR-04-17 | FDA UDI | Class II | Active |
| CranioFit | KT-T9L15H2 | FDA UDI | Class II | Active |
| Bioplate® | P4LL-05-28 | FDA UDI | Class II | Active |
| Bioplate® | 81-3142-CP | FDA UDI | Class II | Active |
| Bioplate® | DBZ3-04 | FDA UDI | Class I | Active |
| Bioplate® | 81-3591[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5901 | FDA UDI | Class II | Active |
| CranioFit | KT-T4L1H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3024[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. |