Identity
- Trade Name
- C-Graft Putty FDA UDI
- Generic Name
- Dental bone matrix implant, human-derived FDA UDI
- Model / Reference
- CG-P30 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809204339402 FDA UDI
- FDA Product Code
- NUN FDA UDI
- GMDN Term
- Dental bone matrix implant, human-derived FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3930 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
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
Category: Dental bone matrix implant, human-derived
C-Graft Putty by Hans Biomed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental bone matrix implant, human-derived.
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- DynaBlast — Keystone Dental Inc. · Class II
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
- Hans Biomed Corporation
Sources (1)
- FDA UDI 29db98f9-8827-4f91-ab8c-532337929af4 32 fields · synced May 30, 2026