Identity
- Trade Name
- TriPore FDA UDI
- Generic Name
- Synthetic bone graft FDA UDI
- Device Name
- TriPore HA in bottle blister, 1-2mm granules, 1.5cc FDA UDI
- Model / Reference
- 1105-1215 FDA UDI
- Description
- TriPore HA in bottle blister, 1-2mm granules, 1.5cc FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05051775000394 FDA UDI
- 510(k) Number
- K070132 FDA UDI
- FDA Product Code
- MQV FDA UDI
- GMDN Term
- Synthetic bone graft FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3045 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
TriPore by Orthogem Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K070132 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Orthogem Ltd
Sources (1)
- FDA UDI 679df93a-0ad8-4447-bcd9-21a0693421e0 35 fields · synced May 31, 2026