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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 17 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | SCP4-14-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-06-05[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE2-03-05 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-04-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3028[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2070-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3481 | FDA UDI | Class I | Active |
| Bioplate® | 81-2017[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3025[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3141[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3584 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L6H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-2068-CP | FDA UDI | Class II | Active |
| Bioplate® | SCE2-04-05 | FDA UDI | Class II | Active |
| Bioplate® | P2BW-04-10 | FDA UDI | Class II | Active |
| Bioplate® | 81-3081 | FDA UDI | Class I | Active |
| Bioplate® | P2LW-04-15 | FDA UDI | Class II | Active |
| Bioplate® | 81-3034-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3414 | FDA UDI | Class I | Active |
| Bioplate® | P2SW-16-63 | FDA UDI | Class II | Active |
| Bioplate® | 81-3031 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L1H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3424 | FDA UDI | Class I | Active |
| Bioplate® | SCD8-04-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-5912 | FDA UDI | Class II | Active |
| Bioplate® | ASB2-45 | FDA UDI | Class I | Active |
| Bioplate® | P8TP-05-14 | FDA UDI | Class II | Active |
| Bioplate® | 81-3107-CP | FDA UDI | Class I | Active |
| Bioplate® | 81-3026-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-3580[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T8L11H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L14H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3595 | FDA UDI | Class II | Unknown |
| Bioplate® | SCD3-03-05[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2001[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T9L12H2 | FDA UDI | Class II | Active |
| Bioplate® | DBP8-04 | FDA UDI | Class I | Active |
| Bioplate® | 81-3045 | FDA UDI | Class I | Active |
| Bioplate® | SCR8-12-01 | FDA UDI | Class II | Active |
| Bioplate® | SCE4-07-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3131-CP | FDA UDI | Class II | Active |
| CranioFit | KT-T1L16H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-4208 | FDA UDI | Class I | Active |
| Bioplate® | 81-3074 | FDA UDI | Class I | Active |
| Bioplate® | P2SW-06-23[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3136 | FDA UDI | Class II | Active |
| Bioplate® | 81-2053 | FDA UDI | Class II | Active |
| Bioplate® | 81-3012 | FDA UDI | Class II | Active |
| Bioplate® | 81-5791[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3363 | FDA UDI | Class I | 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. |