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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 22 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | 81-3055-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3181[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3492 | FDA UDI | Class I | Active |
| Bioplate® | 81-3029[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T2L18H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-09-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-7461 | FDA UDI | Class I | Active |
| Bioplate® | 81-3429 | FDA UDI | Class I | Active |
| Bioplate® | SCD3-03-05 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-04-10 | FDA UDI | Class II | Active |
| Bioplate® | 81-3083 | FDA UDI | Class I | Active |
| Bioplate® | 81-5727[US] | FDA UDI | Class II | Active |
| Bioplate® | ASHA-24 | FDA UDI | Class I | Active |
| CranioFit | KT-T8L12H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3597 | FDA UDI | Class I | Active |
| CranioFit | KT-T1L14H2 | FDA UDI | Class II | Active |
| Bioplate® | P4IP-04-17[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3159 | FDA UDI | Class II | Active |
| Bioplate® | P2SW-24-95 | FDA UDI | Class II | Active |
| Bioplate® | 81-3035 | FDA UDI | Class II | Active |
| Bioplate® | 81-5723-CP | FDA UDI | Class II | Active |
| Bioplate® | ABP4-30 | FDA UDI | Class I | Active |
| Bioplate® | SCD2-05-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-2033 | FDA UDI | Class I | Active |
| Bioplate® | 81-2023 | FDA UDI | Class I | Active |
| Bioplate® | ASHA-25 | FDA UDI | Class I | Active |
| Bioplate® | 81-3585 | FDA UDI | Class II | Active |
| Bioplate® | P2CW-10-37 | FDA UDI | Class II | Active |
| Bioplate® | DBP2-14 | FDA UDI | Class I | Active |
| Bioplate® | P2LW-07-23[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3027[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3592 | FDA UDI | Class II | Active |
| Bioplate® | P4YP-09-45 | FDA UDI | Class II | Active |
| Bioplate® | 81-3349 | FDA UDI | Class II | Active |
| Bioplate® | DBZ4-04 | FDA UDI | Class I | Active |
| Bioplate® | 81-3040[US] | FDA UDI | Class II | Active |
| Bioplate® | P4LR-07-40 | FDA UDI | Class II | Active |
| Bioplate® | 81-3037 | FDA UDI | Class II | Active |
| Bioplate® | P2RW-07-23[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5896 | FDA UDI | Class II | Active |
| Bioplate® | 81-5741[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5722 | FDA UDI | Class II | Active |
| Bioplate® | 81-3528 | FDA UDI | Class II | Active |
| Bioplate® | 81-2079 | FDA UDI | Class II | Active |
| Bioplate® | 81-3034[US] | FDA UDI | Class II | Active |
| Bioplate® | SCD3-06-01 | FDA UDI | Class II | Active |
| Bioplate® | P4LL-07-40 | FDA UDI | Class II | Active |
| Bioplate® | P4ST-16-99 | FDA UDI | Class II | Active |
| Bioplate® | P4TP-06-24 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-10-05 | 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. |