Electrome's Recovery & Rehabilitation program connects FDA-cleared pulsed shortwave therapy infrastructure with modern recovery workflows across musculoskeletal pain, postoperative recovery, physical therapy, sports medicine, and decentralized care.
The program is designed to support a broader shift in healthcare. Recovery is increasingly happening outside the hospital, and patients need non-drug tools that can fit into daily life, provider workflows, and long duration rehabilitation pathways.
Rehabilitation is one of the largest and fastest growing needs in global healthcare. The World Health Organization estimates that approximately 2.4 billion people worldwide are living with a health condition that may benefit from rehabilitation, and that need is expected to increase as populations age and chronic disease burden rises.
In the United States, chronic pain remains a major driver of disability, reduced mobility, and healthcare utilization. CDC data reported that 20.9% of U.S. adults experienced chronic pain in 2021, with high impact chronic pain affecting a meaningful subset of adults and interfering with daily activities.
Electrome's Recovery & Rehabilitation program is focused on areas where bioelectric therapy may fit naturally into existing care pathways:
physical therapy and rehabilitation
orthopedic recovery
sports medicine
chronic musculoskeletal pain
postoperative recovery
home based recovery
non-opioid pain management
connected recovery engagement
Why Recovery Needs New Infrastructure
Traditional recovery pathways often depend on a fragmented mix of in person therapy, medication, home exercises, patient adherence, and follow up visits. That model creates predictable gaps:
patients may not adhere to recovery plans
pain can limit mobility and participation
medication side effects may reduce tolerability
recovery data often remains invisible between visits
providers may lack scalable tools for at home support
"Rehabilitation is not a single encounter, it is a process that unfolds over days, weeks, and months. Our opportunity is to build bioelectric recovery systems that fit into that process, at home, in clinics, and across connected care pathways."
A Continuous, Connected, Personalized Model
Electrome's long term thesis is that recovery infrastructure should become more continuous, connected, and personalized. That means combining wearable therapeutics, provider guided protocols, patient education, recovery engagement, outcomes tracking, AI assisted support, and clinical evidence generation into a single recovery pathway.
Bioelectric Therapy in Rehabilitation
Pulsed Shortwave Therapy (PSWT) uses pulsed electromagnetic fields rather than direct conductive electrical stimulation.
RecoveryRx® is listed by FDA under 510(k) K190251 as a shortwave diathermy device for use other than applying therapeutic deep heat. The FDA 510(k) summary describes RecoveryRx as a pulsed shortwave therapy device using low voltage electronics.
Within recovery and rehabilitation settings, PSWT is relevant because wearable systems may support prolonged use models, low burden therapy application, at home recovery workflows, adjunctive recovery support, and integration with provider directed care.
Published shortwave therapy literature includes studies in musculoskeletal pain and knee osteoarthritis. A 2017 systematic review and meta analysis concluded that short wave therapy was beneficial for relieving pain caused by knee osteoarthritis, while also noting that pulsed modality appeared superior to continuous modality in the analyzed studies.
A separate review of short wave diathermy in musculoskeletal disorders concluded that short wave diathermy may be effective for reducing musculoskeletal pain in the short term, while also emphasizing the need to consider study quality, treatment parameters, and clinical context.
FDA 510(k) ClearedPostoperative PainEdema ReductionClinician-Directed
RecoveryRx® is an FDA 510(k) cleared PSWT device for clinician-directed care, used as an adjunctive therapy for postoperative pain and the reduction of postoperative edema in superficial soft tissue. Available through the Electrome provider program.
Electrome's Recovery & Rehabilitation program is designed for multiple deployment environments.
Physical Therapy. Bioelectric recovery tools may be positioned as an adjunct to exercise, mobility training, and therapist guided rehabilitation.
Orthopedics. Recovery workflows may include musculoskeletal pain, joint recovery, soft tissue recovery, and postoperative support.
Sports Medicine. Wearable recovery systems may support athletes and active adults managing pain, inflammation, and recovery load.
Home Recovery. Long duration wearable systems may help extend recovery support beyond the clinic visit.
Provider Programs. Provider facing workflows may include ordering, patient education, adherence support, and outcomes tracking.
"Recovery happens in motion, not only inside a clinic. Bioelectric therapy is compelling because it can potentially support recovery workflows in a way that is wearable, non-invasive, and compatible with modern rehabilitation pathways."
Commercial Deployment
Recovery & Rehabilitation is a commercial and platform program connected to Electrome's FDA-cleared pain and recovery infrastructure. The deployment model includes:
ActiPatch® consumer recovery products
RecoveryRx® clinical workflows
provider ordering pathways
retailer education
rehabilitation and physical therapy channels
future digital engagement tools
Near-Term Focus, Long-Term Vision
The near term commercial focus remains practical. Make FDA-cleared bioelectric recovery technology easier for patients, providers, and partners to access and use.
The longer term platform vision is broader. Integrate recovery devices, clinical evidence, digital engagement, and outcomes intelligence into a programmable bioelectric medicine infrastructure layer.
Evidence-Aware Positioning
Electrome avoids presenting recovery and rehabilitation as a solved clinical category. The literature around shortwave, pulsed shortwave, and electromagnetic therapy varies by indication, treatment parameters, device design, study population, comparator, endpoint, and exposure duration.
For that reason, the website consistently distinguishes FDA-cleared device status, published clinical evidence, commercial use cases, exploratory pipeline initiatives, and future platform capabilities. This discipline strengthens credibility with providers, regulators, investors, and institutional partners.
This page is provided for scientific and informational purposes only. Recovery & Rehabilitation is a commercial and platform program connected to FDA-cleared pulsed shortwave therapy infrastructure. Statements regarding future platform capabilities, digital workflows, and expanded recovery programs are forward-looking and subject to scientific, clinical, operational, and regulatory uncertainty. No statement on this page should be interpreted as medical advice or as a claim regarding diagnosis, treatment, cure, mitigation, or prevention of disease beyond cleared indications and supported evidence.