Identity
- Trade Name
- Diamodent FDA UDI
- Generic Name
- Dental implant abutment analog, laboratory FDA UDI
- Device Name
- Screw, Titanium Slot FDA UDI
- Model / Reference
- N/A FDA UDI
- Description
- Screw, Titanium Slot FDA UDI
Identifiers
- Catalog Number
- T5240 FDA UDI
- Primary DI / UDI-DI
- D907T52400 FDA UDI
- FDA Product Code
- DZE FDA UDI
- GMDN Term
- Dental implant abutment analog, laboratory FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
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
Category: Dental implant abutment analog, laboratory
Diamodent by Diamodent — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant abutment analog, laboratory.
- Medentika — Medentika GmbH · Class I
- Paltop — Paltop Advanced Dental Solutions, Ltd. · Class I
- Azure — TERRATS MEDICAL SL. · Class I
- AXIOM® — ETABLISSEMENTS ANTHOGYR · Class I
- Azure — TERRATS MEDICAL SL. · Class I
- DYNAMIC ABUTMENT SOLUTIONS — TALLADIUM ESPAÑA SL · Class I
- DYNAMIC ABUTMENT® SOLUTIONS — TALLADIUM ESPAÑA SL · Class I
- Azure — TERRATS MEDICAL SL. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Diamodent
Sources (1)
- FDA UDI ce9f028b-5c08-4f9e-9942-6bbe82736ca0 34 fields · synced Jun 8, 2026