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· Dermal Fillers
SKU 11063

Regenovue SUB-Q

In stock
Volume
1 x 1 mL
Laboratory
NeoGenesis Co., Ltd.
Origin
South Korea
Indication
Deep wrinkles; lip augmentation; structural facial contouring
Trade price and history are verified-only
allpara supplies licensed practitioners. Sign in or apply for a B2B account to see live pricing, volume tiers and price history.

Regenovue SUB-Q - also known as Regenovue Sub Q filler, or Regenovue Sub Q dermal filler - is a dense monophasic cross-linked hyaluronic acid dermal filler by REGENOVUE, designed for deep wrinkles, volume restoration and structural facial augmentation. It is commonly chosen by aesthetic practitioners and clinics for lip augmentation, nose correction, zygoma, chin and forehead augmentation, using lower subcutaneous fat placement for stronger projection and support. The product contains 24 mg/mL cross-linked hyaluronic acid and is intended for professional use only.

Key Benefits of Regenovue SUB-Q

  • Provides volume support for deeper facial correction
  • Suitable for deep wrinkles and structural augmentation
  • Helps improve projection and contour definition
  • Designed for lower subcutaneous fat placement
  • Uses dense monophasic cross-linking technology
  • CE certified
Key Information
Brand Regenovue
Manufacturer NeoGenesis Co., Ltd.
Country of Origin South Korea
Certification CE-certified
Ingredients Cross-linked hyaluronic acid 24 mg/mL; phosphate-buffered saline
Packaging 1 syringe x 1 mL, supplied with 1 x 27G needle and 1 x 25G needle
Use Type Professional, lower subcutaneous fat injection
Injection Depth Lower subcutaneous fat

Indications and Professional Use

Main indications

  • Deep wrinkles
  • Nasolabial folds
  • Lip augmentation
  • Nose correction
  • Zygoma augmentation
  • Chin augmentation
  • Forehead augmentation
  • Structural facial contouring

Professional use

Professional use: For use only by trained medical professionals, administered by injection into the lower subcutaneous fat, following clinical assessment and the manufacturer's instructions for use. Contraindications: Known hypersensitivity to hyaluronic acid. Infection or active inflammation at the treatment site. Injection into blood vessels. Unsuitable anatomical areas without professional assessment.

Treatment areas

  • Lips
  • Nose
  • Zygoma
  • Chin
  • Forehead
  • Nasolabial folds

Patient profile

Patient suitability is determined by the treating practitioner following clinical assessment. Not suitable for patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or anatomical areas assessed as unsuitable by the practitioner.

How Regenovue SUB-Q Works

Regenovue SUB-Q works through a dense, monophasic cross-linked hyaluronic acid gel formulated at 24 mg/mL, designed for stronger projection and structural support when injected into the lower subcutaneous fat. This supports deep wrinkle correction, lip augmentation, and structural facial contouring across areas such as the nose, zygoma, chin and forehead.

Why Order From Allpara

Allpara offers genuine, verified REGENOVUE products from vetted suppliers, with full batch-traceability and expert support. We serve clinics and aesthetic professionals with CE-certified products, fast EU-wide delivery from our EU warehouse, and competitive trade pricing. Our focus is your patients' safety, satisfaction and results - with dedicated after-sales support for your peace of mind.

Frequently Asked Questions

Does Regenovue SUB-Q contain lidocaine?

No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.

How is Regenovue SUB-Q supplied?

Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.

Is Regenovue SUB-Q suitable for lips?

Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.

Where is Regenovue SUB-Q injected?

Regenovue SUB-Q is injected into the lower subcutaneous fat.

Who should not use Regenovue SUB-Q?

Regenovue SUB-Q should not be used in patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or in anatomical areas assessed as unsuitable by the treating practitioner.

/ Specifications

The datasheet

Category
Dermal Fillers
Brand
REGENOVUE
Laboratory
NeoGenesis Co., Ltd.
SKU
11063
Format
1 x 1 mL
Origin
South Korea
Indication
Deep wrinkles; lip augmentation; structural facial contouring
Use
Professional, lower subcutaneous fat injection
/ Product details

The full file

Regenovue SUB-Q - also known as Regenovue Sub Q filler, or Regenovue Sub Q dermal filler - is a dense monophasic cross-linked hyaluronic acid dermal filler by REGENOVUE, designed for deep wrinkles, volume restoration and structural facial augmentation. It is commonly chosen by aesthetic practitioners and clinics for lip augmentation, nose correction, zygoma, chin and forehead augmentation, using lower subcutaneous fat placement for stronger projection and support. The product contains 24 mg/mL cross-linked hyaluronic acid and is intended for professional use only.

NeoGenesis Co., Ltd., country of origin South Korea.

Shipped EU-wide from our EU warehouse, tracked and insured, with 24-72h dispatch. Each unit ships with batch number and expiry, held in EU bond and batch-traceable.

Store to manufacturer specification, away from direct light. Cold-chain is only used where the product requires it.

Net 30 / 60 / 90 day terms* are available to verified accounts on credit approval. Invoicing is supported in EUR, CHF and GBP.

Terms are indicative and confirmed after account review.

Does Regenovue SUB-Q contain lidocaine?

No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.

How is Regenovue SUB-Q supplied?

Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.

Is Regenovue SUB-Q suitable for lips?

Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.

Where is Regenovue SUB-Q injected?

Regenovue SUB-Q is injected into the lower subcutaneous fat.

Who should not use Regenovue SUB-Q?

Regenovue SUB-Q should not be used in patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or in anatomical areas assessed as unsuitable by the treating practitioner.

/ Quick answers

Everything a buyer asks first

Does Regenovue SUB-Q contain lidocaine?
No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.
How is Regenovue SUB-Q supplied?
Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.
Is Regenovue SUB-Q suitable for lips?
Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.
/ FAQ

Frequently asked

No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.
Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.
Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.
Regenovue SUB-Q is injected into the lower subcutaneous fat.
Regenovue SUB-Q should not be used in patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or in anatomical areas assessed as unsuitable by the treating practitioner.

More from NeoGenesis

View laboratory

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Regenovue SUB-Q

In stock
Verified-only pricing
Sign in or apply for a B2B account to see your price.
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Regenovue SUB-Q - also known as Regenovue Sub Q filler, or Regenovue Sub Q dermal filler - is a dense monophasic cross-linked hyaluronic acid dermal filler by REGENOVUE, designed for deep wrinkles, volume restoration and structural facial augmentation. It is commonly chosen by aesthetic practitioners and clinics for lip augmentation, nose correction, zygoma, chin and forehead augmentation, using lower subcutaneous fat placement for stronger projection and support. The product contains 24 mg/mL cross-linked hyaluronic acid and is intended for professional use only.

Key Benefits of Regenovue SUB-Q

  • Provides volume support for deeper facial correction
  • Suitable for deep wrinkles and structural augmentation
  • Helps improve projection and contour definition
  • Designed for lower subcutaneous fat placement
  • Uses dense monophasic cross-linking technology
  • CE certified
Key Information
Brand Regenovue
Manufacturer NeoGenesis Co., Ltd.
Country of Origin South Korea
Certification CE-certified
Ingredients Cross-linked hyaluronic acid 24 mg/mL; phosphate-buffered saline
Packaging 1 syringe x 1 mL, supplied with 1 x 27G needle and 1 x 25G needle
Use Type Professional, lower subcutaneous fat injection
Injection Depth Lower subcutaneous fat

Indications and Professional Use

Main indications

  • Deep wrinkles
  • Nasolabial folds
  • Lip augmentation
  • Nose correction
  • Zygoma augmentation
  • Chin augmentation
  • Forehead augmentation
  • Structural facial contouring

Professional use

Professional use: For use only by trained medical professionals, administered by injection into the lower subcutaneous fat, following clinical assessment and the manufacturer's instructions for use. Contraindications: Known hypersensitivity to hyaluronic acid. Infection or active inflammation at the treatment site. Injection into blood vessels. Unsuitable anatomical areas without professional assessment.

Treatment areas

  • Lips
  • Nose
  • Zygoma
  • Chin
  • Forehead
  • Nasolabial folds

Patient profile

Patient suitability is determined by the treating practitioner following clinical assessment. Not suitable for patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or anatomical areas assessed as unsuitable by the practitioner.

How Regenovue SUB-Q Works

Regenovue SUB-Q works through a dense, monophasic cross-linked hyaluronic acid gel formulated at 24 mg/mL, designed for stronger projection and structural support when injected into the lower subcutaneous fat. This supports deep wrinkle correction, lip augmentation, and structural facial contouring across areas such as the nose, zygoma, chin and forehead.

Why Order From Allpara

Allpara offers genuine, verified REGENOVUE products with full batch-traceability, CE-certified stock, fast EU-wide delivery and expert after-sales support.

Frequently Asked Questions

Does Regenovue SUB-Q contain lidocaine?

No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.

How is Regenovue SUB-Q supplied?

Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.

Is Regenovue SUB-Q suitable for lips?

Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.

Where is Regenovue SUB-Q injected?

Regenovue SUB-Q is injected into the lower subcutaneous fat.

Who should not use Regenovue SUB-Q?

Regenovue SUB-Q should not be used in patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or in anatomical areas assessed as unsuitable by the treating practitioner.

More from NeoGenesis

View laboratory →

Regenovue SUB-Q - also known as Regenovue Sub Q filler, or Regenovue Sub Q dermal filler - is a dense monophasic cross-linked hyaluronic acid dermal filler by REGENOVUE, designed for deep wrinkles, volume restoration and structural facial augmentation. It is commonly chosen by aesthetic practitioners and clinics for lip augmentation, nose correction, zygoma, chin and forehead augmentation, using lower subcutaneous fat placement for stronger projection and support. The product contains 24 mg/mL cross-linked hyaluronic acid and is intended for professional use only.

NeoGenesis Co., Ltd., country of origin South Korea.

Shipped EU-wide from our EU warehouse, 24-72h dispatch, tracked and insured. Each unit ships with batch number and expiry, held in EU bond and batch-traceable. Store to manufacturer specification.

Net 30 / 60 / 90 day terms* for verified accounts on credit approval. Invoicing in EUR, CHF and GBP.

Does Regenovue SUB-Q contain lidocaine?

No. Regenovue SUB-Q is formulated with cross-linked hyaluronic acid and phosphate-buffered saline only. A separate product, Regenovue SUB-Q Plus, is available for buyers who want an anaesthetic-containing version, sometimes marketed as Regenovue Sub-Q Lidocaine.

How is Regenovue SUB-Q supplied?

Regenovue SUB-Q is supplied as a 1 mL syringe with one 27G needle and one 25G needle included.

Is Regenovue SUB-Q suitable for lips?

Yes. Regenovue SUB-Q is indicated for lip augmentation, alongside deep wrinkles, nose correction, zygoma, chin and forehead augmentation.

Where is Regenovue SUB-Q injected?

Regenovue SUB-Q is injected into the lower subcutaneous fat.

Who should not use Regenovue SUB-Q?

Regenovue SUB-Q should not be used in patients with hypersensitivity to hyaluronic acid, infection or active inflammation at the treatment site, or in anatomical areas assessed as unsuitable by the treating practitioner.

* Professional-use product. Packaging may vary by batch or market. Refer to the supplied IFU for full directions and contraindications.