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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 16 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | SCE8-04-05[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T4L18H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-3587 | FDA UDI | Class II | Active |
| Bioplate® | P4TP-06-24[US] | FDA UDI | Class II | Active |
| Bioplate® | SCE8-10-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3078 | FDA UDI | Class I | Active |
| Bioplate® | 81-3567 | FDA UDI | Class I | Active |
| Bioplate® | 81-3486 | FDA UDI | Class I | Active |
| Bioplate® | DBP2-20-SALE | FDA UDI | Class I | Active |
| CranioFit | KT-T1L3H1 | FDA UDI | Class II | Active |
| Bioplate® | P2SB-04-17 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-12-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-5724[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5725-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-5882 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-04-01[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3312 | FDA UDI | Class I | Active |
| Bioplate® | 81-3150 | FDA UDI | Class II | Active |
| Bioplate® | 81-1040 | FDA UDI | Class II | Active |
| Bioplate® | P2NW-06-17[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-2002 | FDA UDI | Class II | Active |
| Bioplate® | 81-3080 | FDA UDI | Class I | Active |
| CranioFit | KT-T9L18H1 | FDA UDI | Class II | Active |
| CranioFit | KT-T3L6H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-5734[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3042 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-04-50 | FDA UDI | Class II | Active |
| Bioplate® | P2CW-08-30[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5900 | FDA UDI | Class II | Active |
| Bioplate® | 81-3141-CP | FDA UDI | Class II | Active |
| Bioplate® | 81-7322 | FDA UDI | Class II | Active |
| Bioplate® | 81-3050-CP | FDA UDI | Class II | Active |
| CranioFit | KT-T8L9H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3066 | FDA UDI | Class I | Active |
| Bioplate® | 81-3181 | FDA UDI | Class II | Active |
| Bioplate® | 81-3521[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-3484 | FDA UDI | Class I | Active |
| Bioplate® | 81-3022-CP | FDA UDI | Class II | Active |
| Bioplate® | DBZ2-04 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-17-05 | FDA UDI | Class II | Active |
| Bioplate® | 81-3053 | FDA UDI | Class II | Active |
| Bioplate® | DBP2-06-SALE | FDA UDI | Class I | Active |
| Bioplate® | P2XP-07-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-5721[US] | FDA UDI | Class II | Active |
| Bioplate® | DBP8-06-SALE | FDA UDI | Class I | Active |
| Bioplate® | P4IP-04-17 | FDA UDI | Class II | Active |
| Bioplate® | 81-3485 | FDA UDI | Class I | Active |
| Bioplate® | 81-3493 | FDA UDI | Class II | Active |
| Bioplate® | P2LW-07-23 | FDA UDI | Class II | Active |
| Bioplate® | P2TB-05-24 | 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. |