Magdent MED (Miniaturized Electromagnetic Device)

Instruction for use:

About (MED)
Magdent’s Miniaturized Electromagnetic Device (MED) technology utilizes an electromagnetic field to stimulate, accelerate, and improve bone formation and quality for shorter and more successful dental implant procedures.
The MED is threaded into the implant like a simple healing abutment. Each MED model is compatible with specific implant models.

Did you Know? 
Magdent’s PEMF forms new blood vessels and reduces proinflammatory cytokines, in addition to increasing the Mesenchymal Stem Cell differentiation to osteoblasts, also in inflammatory condition.
PEMFs increase anti-inflammatory cytokine, such as IL-10 expression, and reduce the expression of the pro-inflammatory cytokine IL-1 and TNF-α.

PEMF Mechanism of Action
The MED enhances the healing process by accelerating osteogenesis 3 times faster around the implant.  It achieves this through a pulsed electromagnetic field that remains active for up to 30 days following a single 3-second activation. With Magdent’s technology, patients can return for full restoration in 30 days for the mandible and 60 days for the maxilla.

Foundations
Same Day Treatment: Use the MED only in case that One Stage Surgery can be performed. Not suitable for immediate loading.

Enhanced Osteogenesis: Producing Pulsed Electro Magnetic Field (PEMF), which has a major effect on osteoblasts, resulting in bone formation even in inflammatory conditions, enhancing the osteogenesis process.

High-risk Patients: By increasing bone volume density, the MED may provide an effective solution for patients with osteoporosis, diabetes, smoking-related bone loss, and cancer-related conditions, ensuring better implant stability and healing.

Temporary Partial Denture: A partial acrylic denture can be used as a temporary solution by designing a recess in its inner surface to fit over the MED, ensuring aesthetic preservation during the healing phase.

Low Pulsed Electromagnetic Field: A precisely controlled low-level current, measured in millitesla (mT), is generated within a 2mm radius around the implant, primarily affecting the upper 7mm of the implant and surrounding soft tissue. Patients do not experience any sensation while the MED is active in their oral cavity.

Indications & Contraindications
Indications: The MED is indicated for all patients undergoing dental implantation. Specially in high-risk patients with decreased bone density and poor bone quality such as patients with osteoporosis, cancer, diabetes, heavy smokers.

Peri-implantitis Treatment: The MED offers significant benefits in managing peri-implantitis and controlling biofilm colonization. PEMF reduces inflammation, enhances soft tissue healing, and promotes bone regeneration, helping prevent and treat periimplantitis. It also reduces harmful biofilm colonization, supporting better implant stability and tissue health. Clinical studies highlight the effectiveness of this approach in improving long-term implant outcomes and minimizing complications.

The enhancement of soft tissue quality strengthens the soft tissue seal, leading to improved bone augmentation outcomes.

Soft Tissue: The MED has demonstrated a beneficial effect on soft tissue, particularly in the formation of keratinized gingiva. In the early healing stages, the soft tissue exhibits weak attachment and continues to reorganize even beyond 60 days. However, with continuous MED use, the soft tissue becomes well structured and maintains close contact with the device, creating a more stable and healthier peri-implant environment. By improving soft tissue integration around implants, the MED supports long-term oral health and enhances implant success.

Contraindications:  The MED should not be used if the implants need to be maintained submerged.

Safety considerations:
• The MED is intended for single use only.
• Don’t sterilized the MED in an autoclave. It will destroy the
electric components and will defect the MED. Each MED is
delivered ready for use, according to the highest standards of
ISO 13845 regulation.
• The safety of the MED in a Magnetic Resonance (MR)
environment has not been evaluated. If a patient requires an
MRI scan, it is recommended to remove the MED prior to
the procedure.

Download Clinical Guidelines, Protocol, Compatibility Deck & Clinical Trials