Is this your brand? Sign in to claim ownership.
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 11 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bioplate® | 81-2020 | FDA UDI | Class I | Active |
| Bioplate® | P4LL-08-40 | FDA UDI | Class II | Active |
| Bioplate® | P2CP-06-23 | FDA UDI | Class II | Active |
| Bioplate® | SCR4-17-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-2005 | FDA UDI | Class II | Active |
| Bioplate® | P2LL-07-23 | FDA UDI | Class II | Active |
| Bioplate® | 81-3055[US] | FDA UDI | Class II | Active |
| Bioplate® | DBZ2-06 | FDA UDI | Class I | Active |
| Bioplate® | 81-2008[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-7304 | FDA UDI | Class II | Active |
| Bioplate® | 81-3149 | FDA UDI | Class II | Active |
| Bioplate® | 81-5902 | FDA UDI | Class II | Active |
| Bioplate® | P2YW-06-18 | FDA UDI | Class II | Active |
| Bioplate® | 81-2072 | FDA UDI | Class II | Active |
| Bioplate® | 81-2056 | FDA UDI | Class II | Active |
| Bioplate® | SCR2-03-01 | FDA UDI | Class II | Active |
| Bioplate® | 81-3376 | FDA UDI | Class I | Active |
| Bioplate® | 81-5733[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T9L6H1 | FDA UDI | Class II | Active |
| Bioplate® | SCE2-04-05[US] | FDA UDI | Class II | Active |
| Bioplate® | P2SW-04-17 | FDA UDI | Class II | Active |
| Bioplate® | SCR8-06-01 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-05-05[US] | FDA UDI | Class II | Active |
| CranioFit | KT-T5L11H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3583 | FDA UDI | Class II | Active |
| Bioplate® | SCD2-03-05 | FDA UDI | Class II | Active |
| Bioplate® | P3BX-04-15 | FDA UDI | Class II | Active |
| Bioplate® | 81-5730 | FDA UDI | Class II | Active |
| CranioFit | KT-T2L10H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L8H2 | FDA UDI | Class II | Active |
| CranioFit | KT-T1L15H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3038 | FDA UDI | Class II | Active |
| CranioFit | KT-T7L3H1 | FDA UDI | Class II | Active |
| Bioplate® | 81-5745[US] | FDA UDI | Class II | Active |
| Bioplate® | 81-5788 | FDA UDI | Class II | Active |
| CranioFit | KT-T1L10H2 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-08-01 | FDA UDI | Class II | Active |
| CranioFit | KT-T6L7H1 | FDA UDI | Class II | Active |
| Bioplate® | P3SB-04-20 | FDA UDI | Class II | Active |
| Bioplate® | P2ST-32-99 | FDA UDI | Class II | Active |
| Bioplate® | 81-3566 | FDA UDI | Class I | Active |
| CranioFit | KT-T9L17H2 | FDA UDI | Class II | Active |
| Bioplate® | 81-3489 | FDA UDI | Class I | Active |
| Bioplate® | SCR4-14-01 | FDA UDI | Class II | Active |
| Bioplate® | SCD3-06-05[US] | FDA UDI | Class II | Active |
| Bioplate® | DBP8-06 | FDA UDI | Class I | Active |
| Bioplate® | 81-2066-CP | FDA UDI | Class II | Active |
| Bioplate® | P2ST-16-63 | FDA UDI | Class II | Active |
| Bioplate® | 81-2007 | FDA UDI | Class II | Active |
| Bioplate® | SCE8-03-05 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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. |