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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 14 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CranioFit | KT-T2L1H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3042[US] | FDA UDI | Class II | Active |
| Bioplate® | P2CP-08-45 | FDA UDI | Class II | Active |
| Bioplate® | 81-2065 | FDA UDI | Class II | Active |
| Bioplate® | 81-2016[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR2-10-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3055 | FDA UDI | Class II | Active |
| Bioplate® | 81-2068 | FDA UDI | Class II | Active |
| Bioplate® | P2SB-02-11 | FDA UDI | Class II | Active |
| Bioplate® | K248-50 | FDA UDI | Class I | Active |
| Bioplate® | SCR8-03-05 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-12-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P2LW-05-21 | FDA UDI | Class II | Active |
| Bioplate® | 81-3061 | FDA UDI | Class I | Active |
| Bioplate® | SCD8-03-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-14-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-5785-CP | FDA UDI | Class II | Active |
| CranioFit | KT-T3L14H2 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-06-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3377 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-09-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-2055 | FDA UDI | Class II | Active |
| Bioplate® | 81-3379-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5745 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-06-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3071 | FDA UDI | Class I | Active |
| Bioplate® | 81-3021 | FDA UDI | Class II | Active |
| Bioplate® | P4ST-08-48 | FDA UDI | Class II | Active |
| Bioplate® | 81-3568 | FDA UDI | Class I | Unknown |
| Bioplate® | P2SW-04-15 | FDA UDI | Class II | Active |
| Bioplate® | P3MC-120 | FDA UDI | Class II | Active |
| Bioplate® | P3XB-06-18 | FDA UDI | Class II | Active |
| CranioFit | KT-T8L13H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3488 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-06-01 | FDA UDI | Class II | Active |
| Bioplate® | P3SB-02-12-05 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-09-05[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE4-05-05[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T7L18H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3064 | FDA UDI | Class I | Active |
| Bioplate® | SCE4-15-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P4LR-04-24 | FDA UDI | Class II | Active |
| Bioplate® | 81-3034 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-04-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3027 | FDA UDI | Class II | Active |
| Bioplate® | 81-3019 | FDA UDI | Class II | Active |
| Bioplate® | 81-3030[US] | FDA UDI | Class II | Active |
| Bioplate® | SCR2-14-01 | FDA UDI | Class II | Active |
| Bioplate® | P2XW-07-17[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3425 | 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. |