Asiga DentaBASE – 385 nm 3D Denture Base Resin Class IIa
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Référence: H104900
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Asiga DentaBASE – Biocompatible denture base 3D resin for digital dentures (385 nm)
Brand : Asiga
Reference / SKU : H104900
Asiga DentaBASE is designed for 3D printing denture bases in a professional dental laboratory.
It supports a reliable digital denture workflow: printed base + teeth (printed, milled, or prefabricated), followed by bonding, characterization, and final polishing.
Denture base
Biocompatible
Class IIa
Class IIa
Wavelength
385 nm
385 nm
Natural pink
Asiga N1
Asiga N1
Stain-resistant
after polish
after polish
Quality
ISO 13485
ISO 13485
Key benefits for the dental laboratory
- High rigidity and strength for stable bases and repeatable batch production.
- Optimized finishing: faster adjustment and efficient polishing on a homogeneous surface.
- Consistent tooth-to-base bonding to help standardize your internal workflow.
- Stain resistance after full polishing for a durable gingival appearance.
- Traceability & quality: manufactured under ISO 13485 to support lab compliance requirements.
Applications (digital denture workflow)
- Full digital denture base production (two-part workflow).
- Bonding with printed teeth, milled teeth, or prefabricated denture teeth.
- Lab standardization: repeatability, fewer remakes, consistent outcomes.
- Lab steps: adjustment, bonding, characterization, final polish.
Printer compatibility & processing
- Printers: 385 nm resin systems (validate your profile per IFU).
- Shade: Asiga N1 (natural pink) – close to a classic gingival tone.
- Post-processing: wash + final cure according to IFU (lab qualification recommended).
- Goal: dimensional stability and a clean surface for consistent tooth bonding.
Videos – Laboratory workflows
Technical specifications
| Material type | Biocompatible dental resin for 3D printing denture bases |
|---|---|
| Indication | Denture base (two-part digital denture workflow) |
| Medical class | Class IIa |
| Shade | Asiga N1 – Natural pink |
| Wavelength | 385 nm |
| Quality / manufacturing | Asiga – ISO 13485:2016 |
Regulatory compliance
- United States: FDA 510(k) cleared.
- European Union: CE marked under MDR.
- Canada: Medical Device Licence (MDL 113395).
- Australia: ARTG 489065.
Documents & resources
Technical FAQ (dental laboratory)
Which lab protocol helps achieve reliable tooth-to-base bonding with DentaBASE?
In the laboratory, reliable bonding starts with a perfectly clean and stable surface.
After printing, follow an effective wash and ensure complete drying before the final cure.
Bonding areas should be prepared in a controlled way to improve retention, without over-abrading or contaminating the surface.
Teeth positioning must be mechanically stabilized during setting to prevent micro-movement that weakens the interface.
Final curing and dimensional stabilization are critical, as they influence rigidity and long-term performance.
To standardize production, validate your “recipe” once (printing + post-processing + bonding), then keep it consistent for all batches.
After printing, follow an effective wash and ensure complete drying before the final cure.
Bonding areas should be prepared in a controlled way to improve retention, without over-abrading or contaminating the surface.
Teeth positioning must be mechanically stabilized during setting to prevent micro-movement that weakens the interface.
Final curing and dimensional stabilization are critical, as they influence rigidity and long-term performance.
To standardize production, validate your “recipe” once (printing + post-processing + bonding), then keep it consistent for all batches.
Why do base rigidity and finishing directly impact patient comfort?
A rigid, homogeneous base limits deformation during insertion and function.
In the lab, this translates into more accurate adaptation and more stable occlusion after tooth setup.
Finishing quality impacts mucosal contact and retention, especially in vestibular and palatal areas.
Progressive, complete polishing reduces surface roughness and improves stain resistance in daily use.
It also boosts productivity, because a surface that finishes cleanly reduces rework and operator time.
In the lab, this translates into more accurate adaptation and more stable occlusion after tooth setup.
Finishing quality impacts mucosal contact and retention, especially in vestibular and palatal areas.
Progressive, complete polishing reduces surface roughness and improves stain resistance in daily use.
It also boosts productivity, because a surface that finishes cleanly reduces rework and operator time.
How can a lab secure 385 nm printer compatibility and post-curing consistency?
385 nm wavelength is the compatibility baseline, but final performance depends on exposure settings and post-curing.
Validate your printer and print profile on test parts before starting batch production.
Useful checks include dimensional stability, surface quality, bonding behavior, and polishing response.
Once validated, keep the same cleaning chain and final cure to avoid variation between batches.
A locked process is the most effective way to reduce returns and standardize quality.
Validate your printer and print profile on test parts before starting batch production.
Useful checks include dimensional stability, surface quality, bonding behavior, and polishing response.
Once validated, keep the same cleaning chain and final cure to avoid variation between batches.
A locked process is the most effective way to reduce returns and standardize quality.
What do Class IIa, MDR, and FDA approvals practically mean for a dental lab?
They provide a documented framework and traceability that help integrate the material into a clinical workflow.
Class IIa indicates a regulatory level suitable for medical use, provided the protocol is followed.
MDR and FDA support international use and quality consistency with demanding prescribers.
For the lab, this helps with audits, material justification, and maintaining a clean technical file.
It is especially relevant when scaling digital dentures and reducing operator-to-operator variability.
Class IIa indicates a regulatory level suitable for medical use, provided the protocol is followed.
MDR and FDA support international use and quality consistency with demanding prescribers.
For the lab, this helps with audits, material justification, and maintaining a clean technical file.
It is especially relevant when scaling digital dentures and reducing operator-to-operator variability.
Asiga DentaBASE – 385 nm 3D Denture Base Resin Class IIa