Identity
- Trade Name
- DiamoDent FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- Ti BASE, Yellow Non-Hexed, 0.35mm Collar, 4.2mm Profile, 6mm Height 3.4mm, BIOMET 3i, Certain Implants FDA UDI
- Model / Reference
- N/A FDA UDI
- Description
- Ti BASE, Yellow Non-Hexed, 0.35mm Collar, 4.2mm Profile, 6mm Height 3.4mm, BIOMET 3i, Certain Implants FDA UDI
Identifiers
- Catalog Number
- AJ1011 FDA UDI
- Primary DI / UDI-DI
- D907AJ10110 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
Category: Dental implant suprastructure, permanent, preformed
DiamoDent by Diamodent — 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
- Diamodent
Sources (1)
- FDA UDI 3175b61d-b873-487f-ae31-cdd0e4d8c32c 34 fields · synced Jun 1, 2026