Identity
- Trade Name
- LuxaPrint Tray FDA UDI
- Generic Name
- Dental impression tray material FDA UDI
- Device Name
- (Meth) acrylate-based light-curing resin for the fabrication of custom impression trays. For DLP/ STL printers at a wavelength of 405 nm or 385 nm. High spirits in 3D. Content: 1 Bottle @ 200 g FDA UDI
- Model / Reference
- 171266 FDA UDI
- Description
- (Meth) acrylate-based light-curing resin for the fabrication of custom impression trays. For DLP/ STL printers at a wavelength of 405 nm or 385 nm. High spirits in 3D. Content: 1 Bottle @ 200 g FDA UDI
Identifiers
- Catalog Number
- 171266 FDA UDI
- Primary DI / UDI-DI
- D9821712660 FDA UDI
- FDA Product Code
- EBH FDA UDI
- GMDN Term
- Dental impression tray material FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3670 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
Category: Dental impression tray material
LuxaPrint Tray by DMG Digital Enterprises SE — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental impression tray material.
- Eazipan LC — VERICOM CO., LTD. · Class I
- INSTANT TRAY MIX POWDER — Lang Dental Manufacturing Company, Inc. · Class I
- Vitacrilic® — FRICKE INTERNATIONAL, INC. · Class I
- Premium Tray — Denplus Inc · Class I
- Bosworth Fastray LC — Harry J. Bosworth Co. · Class II
- OpaTray — OPA DENTAL, LLC · Class I
- DURALAY - BLUE — Reliance Dental Manufacturing · Class I
- SR Ivolen — IVOCLAR VIVADENT AKTIENGESELLSCHAFT · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- DMG Digital Enterprises SE
Sources (1)
- FDA UDI f46b3c6f-76ea-42af-adc7-ef01f41a5d2f 36 fields · synced Jun 8, 2026