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Product Overview
DeneB Classic-S and DeneB Classic-H are Korean cross-linked hyaluronic acid (HA) fillers manufactured by BioPlus Co., Ltd. Both are listed at 20 mg/mL HA in 10 mL prefilled syringes, making gel profile and lidocaine configuration the main specifications to compare when selecting a DeneB Classic product. Classic-S is the more adaptable medium-firm formulation, while Classic-H has a firmer, shape-supportive profile. Both have documented lidocaine and non-lidocaine presentations. Compare the formulation, labeled contents and destination-market authorization before selecting a specific SKU.
Key Features
- Choose between two gel profiles. Classic-S is described as a medium-firm gel, whereas Classic-H is positioned as a firmer, more shape-supportive formulation; the distinction is based on BioPlus product descriptions.
- 20 mg/mL cross-linked hyaluronic acid. Both formulations contain 20 mg of HA per milliliter, corresponding to 200 mg per listed 10 mL syringe.
- 10 mL prefilled presentation. Both Classic variants use one 10 mL syringe per listed commercial pack; the manufacturer's brochure does not list an included needle.
- Select the lidocaine configuration. Documented lidocaine-containing versions are listed at 3 mg/mL (0.3%), while non-lidocaine versions omit this anesthetic. Confirm the exact product's label before purchase or professional use.
- BioPlus MDM and DVS technology. BioPlus identifies DeneB as part of its DVS-cross-linked HA filler range using its proprietary MDM technology platform; this describes manufacturing technology, not proven superiority in clinical outcomes.
Composition & Specifications
| Specification | Details |
|---|---|
| Product Names | DeneB Classic-S; DeneB Classic-H |
| Manufacturer | BioPlus Co., Ltd., Republic of Korea |
| Product Type | Cross-linked hyaluronic acid (HA) injectable filler; medical-device classification subject to applicable jurisdiction |
| HA Concentration | 20 mg/mL in both Classic-S and Classic-H |
| Total HA per Syringe | 200 mg, calculated from 20 mg/mL × 10 mL |
| Cross-linking System | DVS (divinyl sulfone), as described in BioPlus's MDM technology literature |
| Gel Presentation | Cross-linked HA gel in a prefilled syringe |
| Lidocaine Options | With lidocaine: 3 mg/mL (0.3%); without lidocaine: no lidocaine in the listed formulation |
| Syringe Volume | 10 mL |
| Pack Size | 1 prefilled syringe per box, according to specialist supplier listings |
| Needles | Not listed as included in the manufacturer product-brochure specification |
| Manufacturer-Listed Storage | 1–25°C for the DeneB Classic range; follow the exact product carton and instructions for use |
Specifications summarize the manufacturer's DeneB brochure and identified commercial presentations. Lidocaine status, packaging, market authorization and labeling may differ by SKU or destination country.
Understanding the S and H Gel Profiles
Hyaluronic acid is a water-binding component of the extracellular matrix. Cross-linking creates a gel with greater structural persistence than an equivalent non-cross-linked HA solution. The mechanical response of a filler depends on its complete formulation, including its elastic and viscous properties; HA concentration alone cannot determine how firm a product will feel.
BioPlus distinguishes Classic-S and Classic-H primarily through relative gel firmness and contouring behavior. Its proprietary MDM platform incorporates DVS-based HA cross-linking. The manufacturer describes Classic-H as comparatively resistant to deformation, while Classic-S is presented as a less rigid option within the same 10 mL family. These are manufacturer-reported material characteristics, not a guarantee of a specific clinical result, duration or anatomical indication. Lidocaine, where present, is a local anesthetic ingredient and does not define the S/H gel-profile distinction.
Available Formulations: Classic-S, Classic-H, Lido & Non-Lido
Compare the S/H gel profile and lidocaine status as two separate product-selection criteria. The combinations below summarize published formulations; they do not guarantee that each SKU is supplied or authorized in every destination market. TEOSQUARE manages current selectable options, prices and stock separately.
| Formulation | Relative Gel Profile | HA | Lidocaine | Presentation |
|---|---|---|---|---|
| DeneB Classic-S — Non-Lido | Medium-firm; comparatively more adaptable | 20 mg/mL | Not included | 10 mL × 1 syringe |
| DeneB Classic-S — Lido | Medium-firm; comparatively more adaptable | 20 mg/mL | 3 mg/mL (0.3%) | 10 mL × 1 syringe |
| DeneB Classic-H — Non-Lido | Firmer, shape-supportive | 20 mg/mL | Not included | 10 mL × 1 syringe |
| DeneB Classic-H — Lido | Firmer, shape-supportive | 20 mg/mL | 3 mg/mL (0.3%) | 10 mL × 1 syringe |
Published BioPlus materials distinguish certain non-lidocaine CE presentations and lidocaine-containing export presentations. Do not infer that all four listed combinations share the same certificates, labeling or approved indications. Verify each exact SKU and its market-specific IFU.
Professional Product Selection Considerations
When comparing DeneB Classic products for professional procurement, first distinguish Classic-S from Classic-H by their manufacturer-described gel characteristics. Next, verify whether the exact carton is labeled Lido (3 mg/mL lidocaine) or Non-Lido. These are independent specifications: the presence of lidocaine does not identify gel firmness.
- Match the exact product name. Check Classic-S versus Classic-H and confirm the label matches the selected option.
- Verify lidocaine status. Review the original carton and IFU rather than assuming that every market supplies both formulations.
- Confirm contents and storage. Check the listed 10 mL syringe presentation, packaging accessories, expiry date and manufacturer-labeled storage conditions.
- Review authorization for the destination market. Confirm local regulatory status and permitted indications; body-contouring marketing is not proof of approval for any particular anatomical site.
Storage & Handling
BioPlus's product brochure lists a storage temperature of 1–25°C for the DeneB Classic range. Keep products within the conditions stated on their original packaging and comply with the applicable expiration date and market-specific instructions. Do not use a product if its sterile packaging is damaged.
DeneB Classic formulations are injectable medical devices for use by appropriately qualified healthcare professionals. Published promotional materials discuss body contouring, but this does not mean breast, buttock or other large-volume augmentation is authorized in every jurisdiction. In particular, the US FDA advises against injectable dermal fillers for breast or buttock augmentation. Risks associated with filler procedures include infection, nodules, vascular injury and other serious complications. This page does not provide procedural instructions or treatment recommendations.
Frequently Asked Questions
What is the difference between DeneB Classic-S and Classic-H?
Both are BioPlus cross-linked HA fillers containing 20 mg/mL HA in 10 mL syringes. Classic-S is the comparatively less firm, medium-firm option; Classic-H is designed with a firmer gel profile. The comparison describes the manufacturer's formulation characteristics, not interchangeable clinical indications.
Are DeneB Classic-S and Classic-H available with and without lidocaine?
Manufacturer documentation distinguishes non-lidocaine CE presentations and lidocaine-containing export presentations across the Classic range. Supplier listings describe lidocaine at 3 mg/mL (0.3%). Confirm the exact variant and lidocaine status on the product carton before purchase or use.
What should be checked when choosing a DeneB Classic SKU?
Confirm whether the product is Classic-S or Classic-H, its Lido or Non-Lido label, the 10 mL pack contents, storage requirements and the relevant destination-market authorization. TEOSQUARE listing options should be checked against the supplied carton.
How much hyaluronic acid is in a 10 mL DeneB Classic syringe?
At the listed 20 mg/mL HA concentration, a 10 mL syringe contains 200 mg of HA in total. This is an ingredient-content calculation, not a recommended treatment quantity.
What is BioPlus MDM technology?
MDM is BioPlus's proprietary HA filler technology platform, which the company associates with micro-bead monophasic gel design, DVS-based cross-linking and multistage purification. Technology descriptions do not, by themselves, establish clinical superiority or a guaranteed duration.
Are DeneB Classic fillers approved for breast or buttock augmentation?
Approval cannot be assumed from body-contouring marketing. Permitted indications depend on the specific product registration and country. The US FDA has not approved injectable dermal fillers for breast or buttock augmentation and recommends against these uses.