Identity
- Trade Name
- MIS BondBone FDA UDI
- Generic Name
- Synthetic bone graft FDA UDI
- Device Name
- BondBone 0.5cc Bonding-Graft Material FDA UDI
- Model / Reference
- BS-BB005 FDA UDI
- Description
- BondBone 0.5cc Bonding-Graft Material FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290108990072 FDA UDI
- FDA Product Code
- LYC FDA UDI
- GMDN Term
- Synthetic bone graft 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
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
Yes
FDA UDI
Category: Synthetic bone graft
MIS BondBone by MIS Implants Technologies Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- MIS Implants Technologies Ltd.
Sources (1)
- FDA UDI d5be8727-45a7-4c24-9f3f-8b99faba7ac5 33 fields · synced May 31, 2026