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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 6 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | 81-3103-CP | FDA UDI | Class I | Active |
| Bioplate® | 81-3197 | FDA UDI | Class I | Active |
| Bioplate® | 81-3306 | FDA UDI | Class II | Active |
| Bioplate® | 81-3592[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5786 | FDA UDI | Class II | Active |
| Bioplate® | 81-3581[US] | FDA UDI | Class II | Active |
| Bioplate® | P2RW-05-21 | FDA UDI | Class II | Active |
| Bioplate® | 81-5790 | FDA UDI | Class II | Active |
| Bioplate® | DBZ2-04-SALE | FDA UDI | Class I | Active |
| Bioplate® | P8YP-06-17[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3575 | FDA UDI | Class II | Active |
| Bioplate® | 81-3159-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3593 | FDA UDI | Class II | Active |
| Bioplate® | 81-3135 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-10-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P4ZL-04-21 | FDA UDI | Class II | Active |
| Bioplate® | 81-3497 | FDA UDI | Class II | Unknown |
| Bioplate® | DBP8-04-SALE | FDA UDI | Class I | Active |
| CranioFit | KT-T8L17H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T4L12H2 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-04-05 | FDA UDI | Class II | Active |
| Bioplate® | ABP2-30-SALE | FDA UDI | Class I | Active |
| Bioplate® | SCR4-09-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P8XP-07-16 | FDA UDI | Class II | Active |
| Bioplate® | DBP8-14 | FDA UDI | Class I | Active |
| Bioplate® | ABC4-17-SALE | FDA UDI | Class I | Active |
| Bioplate® | 81-7371 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-04-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2080[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2070[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR4-10-01 | FDA UDI | Class II | Active |
| Bioplate® | P3MC-80-99 | FDA UDI | Class II | Active |
| CranioFit | KT-T8L2H1 | FDA UDI | Class II | Active |
| Bioplate® | CPS2-50 | FDA UDI | Class I | Active |
| CranioFit | KT-T4L2H1 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L11H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3577 | FDA UDI | Class II | Active |
| Bioplate® | 81-3591 | FDA UDI | Class II | Active |
| Bioplate® | 81-2077[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5715 | FDA UDI | Class II | Active |
| Bioplate® | P2RW-04-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-3165 | FDA UDI | Class II | Active |
| Bioplate® | 81-3084 | FDA UDI | Class I | Active |
| Bioplate® | 81-7310 | FDA UDI | Class II | Active |
| Bioplate® | 81-5903 | FDA UDI | Class II | Active |
| Bioplate® | 81-2009-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5785[US] | FDA UDI | Class II | Active |
| Bioplate® | P2LW-05-21[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3418 | FDA UDI | Class I | Active |
| Bioplate® | 81-3423 | FDA UDI | Class I | Active |
Related Companies
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Authorities
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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. |