Identity
- Trade Name
- LuxaPost FDA UDI
- Generic Name
- Root canal post, preformed FDA UDI
- Device Name
- Glass fiber-reinforced pre-silanized composite root post. The DMG quality root post. Content: 5 posts (pre-silanized, Ø 1.375 mm ). FDA UDI
- Model / Reference
- 110782 FDA UDI
- Description
- Glass fiber-reinforced pre-silanized composite root post. The DMG quality root post. Content: 5 posts (pre-silanized, Ø 1.375 mm ). FDA UDI
Identifiers
- Catalog Number
- 110782 FDA UDI
- Primary DI / UDI-DI
- EDMG1107820 FDA UDI
- FDA Product Code
- ELR FDA UDI
- GMDN Term
- Root canal post, preformed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3810 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Liquid Chemical FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 1.375 Millimeter FDA UDI
Category: Root canal post, preformed
LuxaPost by DMG Chemisch-Pharmazeutische Fabrik GmbH — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- DMG Chemisch-Pharmazeutische Fabrik GmbH
Sources (1)
- FDA UDI d42d363b-abc7-460f-8453-dc87d56643a9 37 fields · synced May 31, 2026