For Veterinarians & Clinics Patent application filed worldwide Made in Germany

Become a partner in regenerative equine medicine.

Offer your patients an innovative, autologous stem cell therapy—right in your practice. Simple, safe, and fully certified.

EquiCell Maschine – Stammzelltherapie für Pferde

Why choose RegMed for your veterinary clinic?

Position yourself as an innovative hub for regenerative veterinary medicine.

01

Promoting Horse Health

Offer your patients access to regenerative medicine—using the body’s own cells, safe, and with long-lasting results.

02

Modern Practice Positioning

Establish your clinic as a modern, innovative center for cutting-edge veterinary medicine. Your work deserves recognition.

03

Developed with veterinarians – for veterinarians

Designed from the ground up with the clinic in mind. No lab instruments, no bulky equipment, no unnecessary complexity. We’re constantly evolving, together with you.

04

Point-of-Care in 5 Minutes

No lab, no donor horse, no anesthesia. The cell preparation is completed on-site in under 5 minutes.

Indications – When Is the Therapy Suitable?

The concentrate can be administered intra-articularly, intralesionally, or locally in the area of the lesion – depending on the target structure.

01

Osteoarthritis / Degenerative Joint Disease

Suitable

  • Mild to moderate OA (AAEP grade 1–3/5) with mild to moderate radiographic changes
  • Early osteoarthritis after cartilage or subchondral injury as well as after arthroscopic fragment removal
  • Post-traumatic synovitis with early degenerative changes
  • Combination with PRP/IRAP, hyaluronic acid, or NSAIDs possible in moderate OA – especially as an alternative to repeated corticosteroid applications
  • Advanced OA: as an adjunct to standard therapy for pain relief and slowing the process

Less suitable

End-stage OA with severe joint space narrowing, pronounced osteophytes, marked subchondral sclerosis, or mechanical instability; septic arthritis (except as an adjunct with aggressive antimicrobial and surgical treatment).

02

Tendon Injuries

Suitable

  • Acute or subacute SDFT core lesion, preferably within the first 2–8 weeks after injury
  • Mild to moderate lesions (<15–25% cross-sectional area) as well as moderate to severe lesions (25–50%) in performance horses with a high risk of reinjury
  • Selected focal DDFT lesions as well as injuries of the accessory ligament/check ligament with a definable lesion on ultrasound
  • Application intralesional under ultrasound guidance; ultrasound checks every 6–8 weeks mandatory

Less suitable

Complete tears, severe mechanical instability, lesions without an ultrasound-guided placement option, as well as lack of owner compliance for controlled rehabilitation.

03

Ligament Injuries

Suitable

  • Proximal suspensory desmitis (front and hind legs), lesions of the medial or lateral branches of the suspensory ligament
  • Collateral ligament injuries of the interphalangeal joints as well as of the fetlock or carpal joint with a definable lesion
  • Acute and subacute cases preferred; selected chronic cases with active sonographic pathology possible
  • For proximal suspensory desmitis: special care required due to proximity to neurovascular structures
04

Inflammatory Joint Diseases

Suitable

  • Non-septic synovitis, recurrent inflammatory joint effusions, and early-stage degenerative joint disease with synovial inflammation
  • Especially suitable where corticosteroids are contraindicated or should be minimized
  • Possible as part of a multimodal protocol (hyaluronic acid, PRP/IRAP, controlled exercise, hoof correction)
  • Infection must be ruled out before application
05

Postoperative Support / Recovery Promotion

Possible Indications

  • After arthroscopic removal of cartilage debris in the presence of cartilage/synovial inflammation
  • After tendon or ligament injuries, once the lesion is stable and clearly demarcated
  • After focal soft tissue injuries in high-performance sport horses
  • Selected cases after meniscal or soft tissue injuries in the stifle joint
  • Treatment should be integrated into a written rehabilitation plan
06

Further Fields of Application

  • Wound healing and athletic recovery in selected cases
  • Performance support possible in compliance with legal requirements and after case-by-case review
Backed by studies. Transparent in expectations.

Treatment Success & Scientific Basis

A large number of successfully conducted medical studies – both in human medicine and in veterinary medicine – underpin RegMed's treatment approach.

01

Individual Influencing Factors

The specific treatment success depends on a variety of influencing factors. Therefore, the assessment of success is always based on statistical statements – not in the sense of a guarantee for a specific horse.

  • Biological age of the patient
  • Quality and quantity of the cells extracted or injected
  • Concentration of the stem cells
  • Preservation of the habitat
  • Genetic predisposition and pre-existing damage of the patient
02

Recovery Time & Costs

Recovery Time

The recovery time is comparable to that of treatments that only relieve the symptoms.

Costs

The costs for a stem cell treatment with RegMed are within the usual range for comparable treatments.

Financing the Machine

Various financing options are available for financing the required machine.

Our long-standing consulting veterinarian and his internationally active veterinary clinic are already on board. Be one too!

Become a partner now
Science & Technology

The Biology Behind RegMed

The body's own stem cells from adipose tissue – scientifically founded, technologically precise, clinically proven.

200×

more stem cells in adipose tissue than in bone marrow

That's why RegMed relies on adipose-derived stem cells (ADSC) – for higher concentration, gentler extraction, and maximum regenerative power.

01

Pluripotent ADSCs from SVF

The stromal vascular fraction (SVF) contains pluripotent autologous stem cells (ADSC) that can differentiate into almost all tissue types – cartilage, ligaments, muscle, connective tissue. RegMed builds on this finding.

A large number of successfully conducted medical studies underpin the treatment approach
02

Habitat Preserved – Risk Eliminated

RegMed obtains stem cells using purely fluid-mechanical methods – without enzymes, without foreign substances. The cells remain in their natural environment of messenger substances and accompanying cells, which completely eliminates immunological risks.

No immune risk · No donor horse · No foreign cells
03

Patented Filter System

Processing takes place in a special silicone tube with a biodegradable, multi-stage filter system. The closed system is fully sterile and easy to use – directly at the point of care.

CE-certified · Made in Germany · Patent filed worldwide

Why Adipose Tissue – Not Bone Marrow?

The extraction site determines cell quality, concentration, and patient burden. RegMed chooses the superior path.

Bone Marrow
  • Lower stem cell concentration
  • More invasive extraction, higher burden
  • Anesthesia often required
RegMed
Adipose Tissue (ADSC)
  • Up to 200× higher stem cell concentration
  • Minimally invasive extraction at the tailhead
  • Only sedation + local anesthesia required

General treatment procedure

8 clear steps – minimally invasive, fully on-site, without external laboratories.

1
Preparation & warming
Whether on-site or at the veterinary clinic: the required materials are warmed to 39 °C in the RegMed thermal bag 8 hours prior to treatment. The patient receives standard sedation.
2
Disinfection of the collection site
The tail region is thoroughly cleaned and disinfected – in accordance with standard veterinary protocols for maximum procedural safety.
3
Local anaesthesia & minimal incision
Following application of local anaesthesia at the croup, the skin is opened with a minimal incision.
4
Preparation for fat harvesting
Preparation is carried out using the sterile components provided by us – fully hygienic and process-safe.
5
Harvesting & SVF extraction
Via the harvester cannula, warmed saline solution is alternately injected and adipose tissue including the stromal vascular fraction (SVF) is aspirated. Approx. 100 ml are transferred into a storage syringe.
6
Automated cell processing
The storage syringe is inserted into the mobile system. The control of substance flows is fully automated. Cell processing is completed in less than five minutes.
7
Stem cell concentrate ready
Within five minutes at the latest, the stem cell concentrate (approx. 7 ml) can be removed from the filter housing – ready for direct injection or proper storage.
8
Recovery & system immediately ready
While the patient recovers from sedation, the system is immediately ready for use again. In principle, the next treatment can begin straight away.

Advantages over other methods

RegMed combines the highest process safety with maximum convenience – for you and your patients.

CE-certified Made in Germany 5-minute processing
What makes RegMed unique

Point-of-Care Therapy

No external laboratory required.

  • Treatment on-site at the point of care
  • Highest hygienic process safety
  • Simple operating concept
  • Minimally invasive treatment
  • Concentration completed in 5 minutes
  • No anaesthesia required
  • No laboratory required
  • No donor horse required
  • No enzymes required
  • Lasting effect – targeting the root causes
  • Sterility of all components
Become a partner now

Become part of the evolution of equine health

As a partner, you contribute to promoting the well-being of all horses. The development is supported by continuous scientific accompaniment.

Non-binding & free of charge
No risk – we will get back to you within 24 hours.
Scientifically supported
Patented process, CE-certified, Made in Germany.
Already in use across Europe
Many clinics are already relying on this method.

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