Bring Your Pelvic Health
To Its Prime

The MagBelle® AF180 is an FDA-cleared (510(k) K230767) Class II prescription medical device designed for pelvic floor muscle stimulation, rehabilitation, and neuromuscular re-education. It integrates focused electromagnetic stimulation, physician-supervised Kegel biofeedback, and synchronized triggered stimulation in one ergonomic clinical platform.

MagBelle® is designed for healthcare practices including gynecology, urology, urogynecology, physical therapy, and dedicated pelvic health clinics. For patients, it provides non-invasive pelvic floor rehabilitation for individuals experiencing urinary incontinence, postpartum muscle weakness, or loss of core neuromuscular tone.

The system delivers focused electromagnetic energy into the pelvic floor region to induce deep, supramaximal muscle contractions. These contractions stimulate neuromuscular adaptations and muscle conditioning beyond what voluntary Kegel exercises alone can achieve, all while the patient remains comfortably seated and fully clothed.

MagBelle® features three coordinated modalities: (1) Focused Magnetic Stimulation for continuous deep muscle activation, (2) Guided Kegel Biofeedback Training with live pressure waveform feedback for voluntary neuromuscular re-education, and (3) Synchronized Triggered Magnetic Stimulation where electromagnetic pulses fire in response to patient-initiated voluntary contraction thresholds.

Yes, 100% non-invasive. Patients remain fully clothed throughout comfortable 28 to 30 minute sessions without internal probes, skin adhesives, or conductive gels. There is no discomfort and zero downtime, allowing patients to resume normal daily activities immediately following each appointment.

FDA 510(k) clearance (K230767) establishes that the MagBelle® AF180 has met regulatory safety and performance standards as a prescription medical device for pelvic floor muscle stimulation. Emcora Medical is an authorized distributor supporting healthcare providers in adopting this cleared clinical technology.

Yes. Pelvic floor muscle stimulation is designed for both male and female patients. In men, it is widely utilized for post-prostatectomy pelvic floor strengthening and neuromuscular re-education, helping restore continent control following surgical intervention or age-related muscle weakness.

In men, incontinence typically stems from pelvic floor muscle weakness following prostate procedures (such as prostatectomy or TURP), age-related muscle atrophy, neurological conditions, or lifestyle factors. Targeted electromagnetic stimulation reactivates the bulbocavernosus and levator ani musculature to rebuild continent support.

Stress incontinence is treated by physically strengthening the pelvic floor and levator ani muscle density to restore urethral closure pressure during exertion. Urge incontinence is addressed by targeted sacral magnetic stimulation, which helps suppress involuntary detrusor muscle spasms and re-establish proper bladder-brain neural signalling.

Many patients begin reporting noticeable improvements in bladder control after 1 to 3 sessions. Standard clinical protocols generally call for 6 sessions delivered twice weekly over 3 weeks, with progressive muscle conditioning continuing over the weeks following completion.

While primary FDA clearances focus on urinary incontinence and muscle conditioning, deep pelvic floor stimulation activates the levator ani and puborectalis muscles responsible for both urinary and anal sphincter coordination. Strengthening these foundational structures contributes to overall pelvic basin stability.

Yes. Treatments are 100% non-invasive, performed while seated comfortably and fully clothed, without internal probes or discomfort. This makes it ideal for older adults and patients with limited mobility who seek a dignified alternative to invasive procedures.

Practices can schedule an in-clinic evaluation or virtual product demonstration by clicking any Request a Demonstration button or calling (615) 542-9941. An Emcora Medical clinical specialist will coordinate with your team to review device specifications, indications for use, and practice integration workflows.

Emcora Medical coordinates complete end-to-end onboarding: white-glove equipment delivery, on-site or virtual clinical staff protocol training, patient education marketing kits, practice pricing guidance, and ongoing dedicated specialist technical support.