EBI
EBI is a pure-play medical device company that develops FDA-approved electrical bone growth stimulators (PEMF, Capacitive Coupling, and Direct Current) for spinal fusions, fracture nonunions, and failed joint fusions, sold via prescription to neurosurgeons, orthopedic specialists, podiatrists, hospitals, surgery centers, and DME providers in the United States.
- Company typePrivate
- Founded1980
- HeadquartersParsippany, United States
- Headcount1,001–5,000
- GTM typeB2B
- OfferingHardware or Manufacturing
What EBI does
EBI, LLC is a Parsippany, New Jersey-based medical device company founded circa 1980 and currently structured as the only pure-play bone growth stimulation business in the world. The company develops five FDA-approved class III medical devices spanning three electrical stimulation modalities: Pulsed Electromagnetic Field (PEMF, 15Hz, FDA 1979), Capacitive Coupling (CC, 60kHz sinusoidal), and Direct Current (DC). Its non-surgical portfolio includes the Biomet EBI Bone Healing System (PEMF), Biomet OrthoPak (CC), and Biomet SpinalPak (CC); the implantable portfolio includes SpF and EBI OsteoGen, both DC-based devices designed for 24-week in-situ therapy. Reported clinical success rates range from 77% (OrthoPak) to 96% (SpF) across the product line.
The business operates a prescription-based, B2B2C distribution model in which physicians (neurosurgeons, orthopedic specialists, podiatrists) and healthcare institutions (hospitals, surgery centers) prescribe or implant devices, while Durable Medical Equipment providers distribute non-surgical units directly to patients. Reimbursement is sourced from Medicare, Medicaid, workers compensation, and commercial payers; EBI supports this with an in-house reimbursement team handling coding, prior authorization and documentation, plus a Patient Advocacy Group for patient-side logistics. The company maintains a domestic-only (United States) footprint, with manufacturing in Guaynabo, Puerto Rico and headquarters in Parsippany, NJ. Following its May 2025 acquisition by Avista Healthcare Partners and the 2026 acquisition of competitor Xstim, EBI is positioned as the largest standalone pure-play in its therapeutic category, treating over 20,000 patients in 2025.
EBI firmographics
Firmographics- Name
- EBI
- Legal name
- EBI, LLC
- Website
- https://ebibonestimulator.com
- Company type
- Private
- Founded year
- 1980
- Operating status
- Operating
- Headcount range
- 1,001–5,000 employees
- Short description
- EBI is a pure-play medical device company that develops FDA-approved electrical bone growth stimulators (PEMF, Capacitive Coupling, and Direct Current) for spinal fusions, fracture nonunions, and failed joint fusions, sold via prescription to neurosurgeons, orthopedic specialists, podiatrists, hospitals, surgery centers, and DME providers in the United States.
- Ownership category
- akta.pro rank
EBI industry classification
Industry- Product category
- Orthopedic Medical Devices
- NAICS
- Electromedical and Electrotherapeutic Apparatus Manufacturing (334510), Surgical Appliance and Supplies Manufacturing (339113)
- SIC
- Electromedical & Electrotherapeutic Apparatus (3845), Orthopedic, Prosthetic & Surgical Appliances & Supplies (3842)
- akta.pro primary industry
- Rehabilitation Therapy Equipment (PT/OT Modalities, Exercise & Balance Devices) (HLAHAMAG)
- akta.pro secondary industries
- Implantable Neuromodulation & Neurostimulation (SCS/DBS/VNS/PNS) (HLAHAEAK), Spine Implants & Motion Preservation (Fusion/Disc/Interspinous) (HLAHAEAC)
Keywords
Where EBI is headquartered
LocationHeadquarters
- HQ city
- Parsippany
- HQ country
- United States
- HQ region
- North America
Offices2 records
Markets served
EBI business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Supply Chain, Personnel, Technology or R&D, Marketing or Sales, Operations, Infrastructure
Revenue model
- Medical Device Sales - Non-Surgical Bone Growth Stimulators: Sale of FDA-approved non-surgical bone growth stimulation devices including Bone Healing System (PEMF), OrthoPak (Capacitive Coupling), and SpinalPak (Capacitive Coupling). These prescription-only devices are sold to patients through healthcare providers, with insurance reimbursement through Medicare, Medicaid, workers compensation, and commercial healthcare plans.
- Medical Device Sales - Implantable Bone Growth Stimulators: Sale of FDA-approved implantable bone growth stimulation devices including SpF (Spinal Fusion Stimulator) and OsteoGen (Fracture Nonunion Stimulator). These class III medical devices are surgically implanted during procedures and provide around-the-clock stimulation therapy for 24 weeks.
- Insurance Reimbursement and Payer Services: Revenue generated through insurance reimbursement from Medicare, Medicaid, workers compensation, and commercial payers. EBI provides benefit verification, prior authorization assistance, appeals support, and ICD-10/CPT coding guidance as part of their payer services.
Go-to-market motion2 records
Distribution channels3 records
Marketing channels6 records
EBI product offering
Product offeringCore offering
EBI develops, manufactures, and sells FDA-approved bone growth stimulation medical devices that use electrical fields to assist bone healing in spinal fusions, fracture nonunions, failed joint fusions, and congenital pseudarthrosis. The company offers five products across three electrical stimulation technologies: Pulsed Electromagnetic Field (Bone Healing System), Capacitive Coupling (OrthoPak, SpinalPak), and Direct Current implantable devices (SpF, OsteoGen). Devices are prescription-only and sold to healthcare providers, hospitals, surgery centers, and Durable Medical Equipment providers with insurance reimbursement through Medicare, Medicaid, workers compensation, and commercial payers.
Product overview
EBI offers a complete portfolio of bone growth stimulation products consisting of both non-invasive and implantable medical devices. The non-surgical portfolio includes the Biomet® EBI® Bone Healing System (PEMF technology), Biomet® OrthoPak® (Capacitive Coupling), and Biomet® SpinalPak® (Capacitive Coupling). The implantable portfolio includes SpF® Implantable Spinal Fusion Stimulators and EBI® OsteoGen™ (both using Direct Current technology). These products work through distinct electrical stimulation technologies—PEMF, Capacitive Coupling, and Direct Current—to promote bone healing in nonunion fractures, failed fusions, and as adjuncts to spinal fusion surgery.
Differentiator
Problem solved
Functional benefit
Brands
- Biomet EBI Bone Healing System: FDA-approved non-invasive bone growth stimulation device using Pulsed Electromagnetic Field (PEMF) technology for treatment of nonunion fractures, failed fusions, and congenital pseudarthrosis.
- Biomet OrthoPak
- Biomet SpinalPak
- SpF Implantable Spinal Fusion Stimulators
- EBI OsteoGen
Products and services
- Biomet EBI Bone Healing System FDA-approved non-invasive bone growth stimulation device using Pulsed Electromagnetic Field (PEMF) technology at 15Hz as adjunctive therapy for nonunion fractures, failed fusions, and congenital pseudarthrosis. Delivers stimulation through flexible treatment coils providing 360-degree coverage.
- Biomet OrthoPak Non-invasive Bone Growth Stimulator System FDA-approved non-invasive bone growth stimulator using 60kHz Capacitive Coupling (CC) technology delivered via Soft-Touch electrodes for treatment of established fracture nonunions.
- Biomet SpinalPak Non-invasive Spine Fusion Stimulator System FDA-approved non-invasive spine fusion stimulator using Capacitive Coupling (CC) technology as adjunctive therapy for lumbar spinal fusion surgery.
- SpF Implantable Spinal Fusion Stimulators FDA-approved class III surgically implanted battery-powered direct current (DC) bone growth stimulation device featuring titanium cathode design, designed to promote bone healing following spinal fusion surgery with constant around-the-clock therapy for 24 weeks.
- EBI OsteoGen Surgically Implanted Bone Growth Stimulators FDA-approved class III surgically implanted battery-powered direct current (DC) bone growth stimulation device (20µA single-lead, 40µA dual-lead) for treatment of fracture nonunions, providing constant around-the-clock therapeutic treatment for 24 weeks.
Quantifiable outcome
- SpF stimulator achieved 96% overall (clinical and radiographic) success rate in instrumented lumbosacral fusions
- +5 more outcomes
Companies that use EBI
Customer profileSegments6 records
Ideal customer profiles4 records
EBI technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature6 records
EBI partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- XstimcoreEBI acquired Xstim, strengthening its market leadership and reinforcing its position as the only pure-play bone growth stimulation company. The acquisition expands EBI's product portfolio and customer base in the bone growth stimulation market. Xstim was a competitor in the bone growth stimulation space with products including the Xstim Spine Fusion Stimulator.
Scale indicators10 records
Recent moves6 records
Expansion highlights5 records
EBI competitors and assessment
Company assessmentBroad incumbents
- Medtronic: Medtronic's Spine and Biologics division is a global spine surgery leader and a major customer-adjacent player for EBI, since spinal fusion procedures generate demand for EBI's SpF and SpinalPak stimulators. EBI's CEO previously held senior sales leadership at Medtronic Spine and Biologics for nine years.
- Stryker: Stryker is a broad medical device incumbent with deep spine, orthopedic trauma, and surgical franchises that compete with EBI in the operating room channel for implantable bone growth stimulators. Its scale and hospital purchasing relationships shape the broader orthopedic environment in which EBI sells its SpF and OsteoGen devices.
- Globus Medical: Globus Medical (which merged with NuVasive) is one of the largest spine-focused medical device companies, providing fusion hardware and biologics used in the same spinal fusion procedures where EBI's SpF and SpinalPak serve as adjunctive electrical stimulation therapy. Overlap in spine surgeon customer base is substantial.
- Smith+Nephew: Smith+Nephew operates across orthopedic reconstruction, trauma, and sports medicine with a meaningful presence in bone healing adjacencies. While not a direct bone growth stimulator peer, it competes for orthopedic specialist mindshare and DME channel relationships that EBI depends on.
- Zimmer Biomet: Zimmer Biomet is a global orthopedic and surgical implant leader whose "Biomet" brand appears on several EBI product names (Biomet EBI Bone Healing System, Biomet OrthoPak, Biomet SpinalPak). Zimmer Biomet operates broadly in spine, trauma, and reconstructive orthopedics, making it both a former parent and a continuing adjacent incumbent.
Direct peers
- Bioventus: Bioventus competes directly with EBI in the bone healing adjunct category through its EXOGEN ultrasound bone healing system, targeting the same fracture nonunion and fusion indications. Both companies sell through orthopedic specialists, podiatrists, and DME channels with similar reimbursement dynamics.
- Orthofix Medical: Orthofix Medical is the closest direct competitor to EBI in bone growth stimulation, offering Cervical-Stim and Spinal-Stim implantable stimulators as well as the Physio-Stim for nonunions. EBI's new CEO Kevin Kenny was previously President of Global Spine at Orthofix, underscoring the overlap in product portfolio, customer base (spine surgeons), and clinical positioning.
- DJO (Enovis): DJO, now part of Enovis, markets bone growth stimulation products (e.g., CMF OL1000 and related bone healing devices) directly competing with EBI's OrthoPak and SpinalPak capacitive coupling devices. Both sell through orthopedic and podiatric channels with similar DME distribution models.
Others
- B. Braun/Aesculap: B. Braun, through its Aesculap division, provides orthopedic surgical implants and devices used in spinal fusion and trauma procedures. It is an adjacent ecosystem participant rather than a direct stimulator competitor, but EBI's CEO previously held senior sales leadership at B. Braun/McGaw, indicating operational familiarity.
Emerging players
- Collagen Solutions (or other emerging regenerative/biologic bone healing players): Emerging regenerative and biologic bone healing companies (e.g., Regenexx, mesoblast-adjacent therapies, novel BMP formulations) target the same spinal fusion and nonunion indications as EBI's electrical stimulators. These emerging modalities represent a long-term competitive vector that could erode EBI's adjunctive therapy share if clinical evidence matures.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
EBI financial estimates
Financial estimateRevenue estimate
Valuation estimate
EBI leadership team
Management profileNumber of profiles
Profiles2 records
EBI subsidiaries and ownership
Company hierarchySubsidiaries1 record
EBI funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
EBI M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about EBI
What does EBI do?
EBI develops, manufactures, and sells FDA-approved bone growth stimulation medical devices that use electrical fields to assist bone healing in spinal fusions, fracture nonunions, failed joint fusions, and congenital pseudarthrosis. The company offers five products across three electrical stimulation technologies: Pulsed Electromagnetic Field (Bone Healing System), Capacitive Coupling (OrthoPak, SpinalPak), and Direct Current implantable devices (SpF, OsteoGen). Devices are prescription-only and sold to healthcare providers, hospitals, surgery centers, and Durable Medical Equipment providers with insurance reimbursement through Medicare, Medicaid, workers compensation, and commercial payers.
Is EBI a public or private company?
EBI is a private company. It is classified as private equity controlled and is currently operating.
When was EBI founded?
EBI was founded in 1980. It employs 1,001 to 5,000 people.
Where is EBI based?
EBI is headquartered in Parsippany, United States, in the North America region.
How does EBI make money?
Three revenue lines are on record. Medical Device Sales - Non-Surgical Bone Growth Stimulators are the primary driver. The others are medical Device Sales - Implantable Bone Growth Stimulators and insurance Reimbursement and Payer Services.
Who are EBI's main competitors?
Broad incumbents on record are Medtronic, Stryker, Globus Medical, Smith+Nephew and Zimmer Biomet. Direct peers are Bioventus, Orthofix Medical and DJO (Enovis). B. Braun/Aesculap is listed as an others. Collagen Solutions (or other emerging regenerative/biologic bone healing players) is listed as an emerging player.
Does EBI have an API?
No public API is recorded for EBI.
What industry is EBI in?
EBI's product category is Orthopedic Medical Devices. Its primary akta.pro industry code is HLAHAMAG, Rehabilitation Therapy Equipment (PT/OT Modalities, Exercise & Balance Devices), with a secondary code of HLAHAEAK, Implantable Neuromodulation & Neurostimulation (SCS/DBS/VNS/PNS). Its NAICS code is 334510 and its SIC code is 3845.