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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 12 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | 81-3161[US] | FDA UDI | Class II | Active |
| Bioplate® | SCD2-06-05 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L5H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3581 | FDA UDI | Class II | Active |
| Bioplate® | 81-2066 | FDA UDI | Class II | Active |
| Bioplate® | P2CP-04-15 | FDA UDI | Class II | Active |
| CranioFit | KT-T9L13H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-2072[US] | FDA UDI | Class II | Active |
| Bioplate® | P1MC-36-43 | FDA UDI | Class II | Active |
| Bioplate® | 81-5770 | FDA UDI | Class II | Active |
| Bioplate® | P2XW-07-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-3138 | FDA UDI | Class II | Active |
| Bioplate® | 81-5743-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3361 | FDA UDI | Class I | Active |
| Bioplate® | P4LL-04-24 | FDA UDI | Class II | Active |
| Bioplate® | 81-3582 | FDA UDI | Class II | Active |
| CranioFit | KT-T5L14H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3580 | FDA UDI | Class II | Active |
| Bioplate® | 81-3035[US] | FDA UDI | Class II | Active |
| Bioplate® | P4SK-04-28 | FDA UDI | Class II | Active |
| Bioplate® | SCD8-05-01 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-12-01 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-04-01 | FDA UDI | Class II | Active |
| Bioplate® | P2LW-04-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-2026 | FDA UDI | Class I | Active |
| Bioplate® | 81-3060[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T2L9H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3021-CP | FDA UDI | Class II | Active |
| Bioplate® | P8CP-08-29 | FDA UDI | Class II | Active |
| Bioplate® | 81-2024 | FDA UDI | Class I | Active |
| Bioplate® | 81-3148[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3184-CP | FDA UDI | Class II | Active |
| CranioFit | KT-T5L6H1 | FDA UDI | Class II | Active |
| Bioplate® | P3CP-08-45 | FDA UDI | Class II | Active |
| Bioplate® | P2TB-05-19 | FDA UDI | Class II | Active |
| CranioFit | KT-T5L18H1 | FDA UDI | Class II | Active |
| Bioplate® | P4YP-05-22 | FDA UDI | Class II | Active |
| Bioplate® | P2MC-120 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-08-01 | FDA UDI | Class II | Active |
| Bioplate® | DBP8-10-SALE | FDA UDI | Class I | Active |
| Bioplate® | 81-2012[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3022 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-08-01 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-13-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3033 | FDA UDI | Class II | Active |
| Bioplate® | 81-2047[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3573 | FDA UDI | Class II | Active |
| Bioplate® | 81-3054[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE4-13-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-5730-CP | FDA UDI | Class II | 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. |