This page lists the categories I source for licensed clinics in the European Union, in the order of my current focus. For each one it explains how the products are regulated. It also states what I do not supply.
There are no prices here and no ordering function. I buy against confirmed orders and hold no stock. Availability and price are confirmed for each request, after I have checked your professional status and the rules of your country. How an order works, shipping costs and delivery times are on the Payment and delivery page.
Certificates
Before I quote a product, I check its certificate. Where the manufacturer holds a certificate under Regulation (EU) 2017/745 (MDR), I quote on that basis. Some devices are still lawfully on the market under a certificate issued under the old directives, during the transition set by Regulation (EU) 2023/607. For those, the quotation says so and gives the end date. From 1 January 2028, I quote Class III injectables only with an MDR certificate.
Product categories
Before the categories
Classification is not uniform across the Union. A product that is a CE-marked device in one member state can be a medicinal product in another. I check the status in your country before I quote, and I decline where the product would not be lawful in your hands.
The names below are products I can source inside the EU and quote on request.
Categories
- Biostimulators
- Polynucleotides
- Skin boosters
- Hyaluronic acid fillers
- Threads
- Procedure consumables and sutures
- Mesotherapy
- Hair and scalp
- Injectable lipolysis
- Exosome and conditioned-media products
Biostimulators
Biostimulators work through the patient’s own collagen response. Results build over weeks, not at the moment of injection, which is why they belong in longer treatment plans.
Poly-L-lactic acid (PLLA): Sculptra (Galderma) · Lanluma (Sinclair)
Calcium hydroxylapatite (CaHA): Radiesse · Radiesse (+) Lidocaine (Merz Aesthetics)
Hyaluronic acid with CaHA: HArmonyCa with Lidocaine (Allergan Aesthetics)
Polycaprolactone (PCL): Ellansé (Sinclair) · GOURI (DEXLEVO)
Regulation. Class III medical devices.
Handling. Supplied only in original, sealed packaging. Reconstitution, where required, follows the manufacturer’s instructions for use.
A note on price. This is the category counterfeiters target most. A price far below the European professional level is a warning sign, not a bargain.
Polynucleotides
Highly purified polynucleotides support the skin’s own repair processes. Formulations differ in concentration and in whether hyaluronic acid is added.
PLINEST · PLINEST fast · PLINEST ONE · PLINEST Body · NEWEST · NEWEST One (Mastelli)
PolyPhil (Croma-Pharma)
Nucleofill (Promoitalia)
Regulation. Class III medical devices in most member states. National interpretation has changed over time. If your authority treats a specific preparation as a medicinal product, I do not supply it to your market.
Handling. Storage and transport follow each product’s instructions for use. Where refrigeration is required, the quotation states how the goods travel.
Skin boosters
These products work on hydration, elasticity and skin quality rather than volume, and are often combined with biostimulators.
Profhilo · Profhilo Structura · Viscoderm (IBSA)
Restylane Skinboosters (Galderma)
Jalupro Classic · Jalupro HMW · Jalupro Super Hydro · Jalupro Young Eye (Professional Derma)
Kytogen (Sinclair)
NCTF 135 HA (Fillmed)
Regulation. Medical devices; the class depends on composition and intended use.
Handling. Several have a shorter shelf life than volumising fillers. Every unit still arrives with at least twelve months remaining.
Hyaluronic acid fillers
Hyaluronic acid remains the base of daily practice: different gel textures, injection depths and indications, from fine lines to volume and structural support.
Restylane (Galderma) · Juvéderm (Allergan Aesthetics) · Belotero (Merz Aesthetics) · Teosyal RHA (Teoxane) · STYLAGE (Vivacy) · saypha (Croma-Pharma) · Aliaxin (IBSA) · ART FILLER (Fillmed)
Regulation. Injectable fillers are Class III devices. Fillers placed on the market for a purely aesthetic purpose also fall under Annex XVI of the MDR and the common specifications in Implementing Regulation (EU) 2022/2346, applicable since 22 June 2023.
Handling. Ambient transport. Storage as stated in the instructions for use, protected from light and frost.
Threads
Thread lifting is technique-sensitive, and consistency between batches matters more here than in most categories.
PDO threads: cog · mono · screw · twin
Suspension threads: Silhouette Soft (Sinclair)
Regulation. Sterile, single-use, Class III devices.
Handling. Sterile packaging must be intact on arrival.
Procedure consumables and sutures
For the injection work itself and for clinics that perform minor surgical procedures: cannulas, needles and sutures from manufacturers such as Ethicon, B. Braun, Resorba, SMI and Assut Europe. The same sourcing and traceability rules apply as for injectables.
Regulation. Medical devices, Class I to Class III depending on the product.
Mesotherapy
Protocols vary widely: hyaluronic acid preparations, vitamin and amino acid complexes, peptides and similar formulations, from manufacturers such as Fillmed, Revitacare, Toskani and Sunekos.
Regulation. Mixed. The composition decides the classification, and it differs between member states. Some products are devices across the Union; others are medicinal products in certain countries. I check the status for your market before I quote.
Hair and scalp
Formulations for scalp and follicle support are requested by dermatology practices and aesthetic clinics alike, for example Jalupro Classic, whose manufacturer includes hair strengthening among its uses, and DR.CYJ Hair Filler (Caregen).
Products presented as pharmacological treatments for hair loss are medicinal products and fall outside what I supply.
Injectable lipolysis
Preparations for the localised reduction of fat, such as Aqualyx and Alidya (Marllor Biomedical) and Prostrolane (Caregen).
Regulation. Tightly regulated and inconsistent across the Union. Some lipolytic preparations hold CE device status. Formulations based on phosphatidylcholine or deoxycholic acid can be authorised medicinal products in some countries and unlicensed in others. I supply only where the product holds device status in your country, so answers in this category take longer.
Lemon Bottle. I do not supply it. In March 2024, Swissmedic classified it as an illegal medicinal product. Its laboratory found that samples from different sources did not match the declared ingredients; in one sample, none of the listed ingredients was detected.
Exosome and conditioned-media products
Products described as exosomes are widely marketed in aesthetics. In the European Union, a preparation of biologically active vesicles intended for injection falls, in most cases, under medicinal-product law, and these products generally hold no such authorisation. I source this category only for topical, post-procedure use, and only where the product is lawfully marketed as a cosmetic or a device in your country.
What I do not supply
Botulinum toxin. It is a medicinal product, not a device. Supplying it requires a wholesale distribution authorisation for medicinal products, which I do not hold.
Injectable hyaluronidase. It is a medicinal product.
Exosome preparations for injection.
Anything classified as a medicinal product in your country, even if the same product is a device elsewhere in the Union.
Anything I cannot trace to an identified supplier inside the EU. If I cannot document where it comes from, I do not offer the product, whatever the margin.
Traceability under Article 25 of the MDR
Counterfeit and grey-market injectables remain a real problem in this sector. Every product I source comes from a supplier inside the European Union: the manufacturer, one of its authorised distributors, or a wholesaler they supply. For each order, I can identify the economic operator who supplied me, as Article 25 of the Regulation requires. Where I buy directly from the manufacturer, I can show you the documentation. Where I buy from a distributor or a wholesaler, I name the supplier of your order on request, but I cannot show you the manufacturer’s authorisation for every brand.
The lot number, expiry date and device identifier (UDI) are on the packaging and recorded against your order, so you can check the device and its manufacturer in EUDAMED yourself.
On arrival
Every unit arrives with at least twelve months of shelf life remaining. If sterile packaging is damaged, photograph it and tell me within 48 hours; I will replace the product or refund it.
How the list grows
Added only once the supply route exists
This page does not list every aesthetic brand sold in Europe, and that is deliberate. A name is added when I have a documented supply route for it inside the EU, and removed when I no longer do.
If what you need is not listed, ask. The same checks apply, and you will get a clear answer, including when the answer is no.
Product names on this page are trademarks of their respective owners. MaxMed Systems is an independent supplier. It is not a manufacturer and is not affiliated with, or appointed by, the manufacturers named here.