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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 18 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | 81-3079 | FDA UDI | Class I | Active |
| Bioplate® | 81-3578[US] | FDA UDI | Class II | Active |
| Bioplate® | P2YP-06-18 | FDA UDI | Class II | Active |
| Bioplate® | ADG5-01 | FDA UDI | Class I | Unknown |
| Bioplate® | SCR2-03-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3049 | FDA UDI | Class II | Active |
| Bioplate® | P4HP-08-26 | FDA UDI | Class II | Active |
| Bioplate® | 81-3138-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5770[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5724-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5788[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5744 | FDA UDI | Class II | Active |
| Bioplate® | 81-2018 | FDA UDI | Class I | Active |
| Bioplate® | P4XP-06-26 | FDA UDI | Class II | Active |
| Bioplate® | 81-3025 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-06-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-07-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-5887 | FDA UDI | Class II | Active |
| Bioplate® | CPS8-50-SALE | FDA UDI | Class I | Active |
| Bioplate® | 81-2011 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-14-05 | FDA UDI | Class II | Active |
| Bioplate® | AMB3-30 | FDA UDI | Class I | Active |
| Bioplate® | 81-5915 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L1H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3352 | FDA UDI | Class II | Active |
| Bioplate® | 81-3023[US] | FDA UDI | Class II | Active |
| Bioplate® | CPS4-50-SALE | FDA UDI | Class I | Active |
| Bioplate® | P2RW-04-13 | FDA UDI | Class II | Active |
| Bioplate® | P2MC-82-97[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2076[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3138[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T4L13H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-2049[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3036-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-2047CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3037[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T3L4H1 | FDA UDI | Class II | Active |
| Bioplate® | ABC3-10 | FDA UDI | Class I | Active |
| Bioplate® | SCR8-04-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3496 | FDA UDI | Class II | Unknown |
| Bioplate® | 81-2081 | FDA UDI | Class II | Active |
| Bioplate® | 81-7307 | FDA UDI | Class II | Active |
| Bioplate® | 81-3020[US] | FDA UDI | Class II | Active |
| Bioplate® | DBZ4-06 | FDA UDI | Class I | Active |
| Bioplate® | P4CP-08-45[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2003 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L6H1 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-04-50 | FDA UDI | Class II | Active |
| Bioplate® | 81-5728-CP | FDA UDI | Class II | Active |
| Bioplate® | SCR2-06-05 | FDA UDI | Class II | Active |
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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. |