BioReg vs Curatron: Specification Comparison

    Curatron sells two different PEMF technologies to clinics, oscillating and impulse, and publishes detailed specifications for both. BioReg publishes closed-loop biofeedback on its top tiers. This page sets the published figures side by side and does not decide which approach is better, because Curatron does not either.

    “Which PEMF technology is better for what, remains an open question.”

    Curatronic Ltd., on its own models page. Source

    Curatron figures sourced from Curatronic’s own published material, verified September 2026. Scope is their clinical line: PC Super, Ultra Power 3D, Premium-Flash and Ultra-Flash.

    BioReg

    BioReg builds low-intensity PEMF and bioregulation systems for licensed practitioners and home users, from the Nesta home line through the Nesta Pro practitioner system, the SanoCenter multi-station clinic platform, and the CellCom closed-loop flagship, which reads two input channels during a session and adjusts output in response.

    Source: BioReg specification matrix

    Curatron

    Curatronic Ltd. publishes two separate technologies. The oscillating models, which they describe as “true” PEMF, include the PC Super and the Ultra Power 3D. The impulse models, branded Flash, include the Premium-Flash and the Ultra-Flash. Their material states that most doctors buy either the Ultra-Flash, the 3D system, or both. Two further models, the XPSE and the Multi-Flash, are published as spanning home and small clinical use and sit outside this comparison.

    Source: Curatronic, Curatron PEMF models

    Oscillating or impulse: what Curatron publishes about the split

    Curatron is the only manufacturer in this comparison set that sells both approaches, which makes their written position on the difference worth reading directly. On the impulse side they state that “each individual high intensity impulse will go fully through the body,” that the pulses are “shorter in duration” than oscillating output, and that “the quantity of energy transferred by each pulse into the body is different from oscillating technology.”

    On the oscillating side they state that “if looking exclusively for energy medicine like energizing the body, one might tend to opt for oscillating technology,” while noting that “full body penetration is less than with Flash technology.” They also disclose a side effect of the impulse line: “muscle contractions might occur in high settings.”

    Two manufacturer positions on how to measure output sit side by side in this category. Pulse PEMF publishes no gauss figure and argues that gauss is not the meaningful number, pointing instead to how fast the field changes. Curatron publishes both gauss maxima and a pulse rise time of 140 micro seconds, and argues from the quantity of energy transferred per pulse. Both are manufacturers describing their own design philosophy. This page does not adjudicate between them.

    The background on those two approaches, including what published research does and does not establish about intensity, is set out in high-intensity vs low-intensity PEMF. BioReg systems are low-intensity.

    Source: Curatronic, Curatron PEMF models

    How do the published specifications compare?

    Every Curatron cell is cited to Curatronic’s own published material and is reproduced in the units they publish. Where Curatron does not publish a figure, the cell says so.

    Specification comparison of the BioReg device line and the Curatron clinical line
    SpecificationCuratron clinical lineBioReg device line
    Field intensity, oscillating modelsPC Super: up to 100 milli Tesla (1000 Gauss) with the very high energy coil. Ultra Power 3D: 50 milli Tesla (500 Gauss) simultaneously over the main area of the 3-D mattress; the unit drives one 50 milli Tesla 3-D mattress or two 15 milli Tesla high power mattresses.Source: Curatronic, Curatron PC SuperSource: Curatronic, Curatron Ultra Power 3D100+ µT across the line.
    Source: BioReg specification matrix
    Field intensity, impulse modelsPremium-Flash: maximum intensity up to 7000 Gauss = 700 milli Tesla = .7 Tesla. Ultra-Flash: up to 10.000 Gauss (LITE up to 7.000 Gauss, PLUS up to 13.000 Gauss). Published as unit maxima, not per applicator.Source: Curatronic, Curatron Premium-FlashSource: Curatronic, Curatron Ultra-Flash100+ µT across the line.
    Source: BioReg specification matrix
    Published frequency or pulse rateOscillating line: Curatron PC published with a frequency range between 1 and 50 Hz. Impulse line: pulse rate published per model, Premium-Flash < 1 to 7.8 pulses per second, Ultra-Flash < 1 to 5 pulses per second.Source: Curatronic, Curatron PC SuperSource: Curatronic, Curatron Premium-FlashSource: Curatronic, Curatron Ultra-FlashCellCom 1 Hz to 1 MHz; SanoCenter 1 Hz to 200 kHz; Nesta Pro 0.5 Hz to 30 Hz.
    Source: BioReg specification matrix
    Waveform and pulse characteristicsImpulse line: waveform impulse, pulses of around one milli second, with a rise time of 140 micro seconds. No waveform is named for the oscillating models.Source: Curatronic, Curatron PEMF modelsSource: Curatronic, Curatron Premium-FlashNot published.
    Source: BioReg specification matrix
    Programs and protocolsEach Curatron unit has 10 built-in therapy programs. On PC Super and Ultra Power 3D, therapy settings can also be selected from a PC software database containing “almost one hundred ready for use therapy protocols,” with the full protocol list offered as a download.Source: Curatronic, PEMF therapy programsSource: Curatronic, Curatron PC Super553 CellCom, 142 SanoCenter, 48 Nesta Pro.
    Source: BioReg specification matrix
    Protocol editingOscillating software: selectable frequencies from 1 to 50 Hz, intensity steps from 20 to 150 percent, stage time 1 to 20 minutes, total program up to 99 minutes. Flash software: each stage programmed between 1 and 20 minutes, total for all stages 99 minutes.Source: Curatronic, PEMF therapy programsSource: Curatronic, Curatron Ultra-FlashNesta Pro practitioner-editable in the device interface.
    Source: BioReg specification matrix
    ApplicatorsOscillating: therapy pad, full body mattress, High Energy Coil (Type A), Very High Energy Coil (Type B), travel mat, 3D mattress, butterfly coil, switch box for two applicators. Flash: loop coil, figure 8 coil, pad, medium mat, full body mat. The Ultra-Power 3-D unit has 2 outputs for two applicators working at the same time, and the Ultra-Flash has a dual applicator feature.Source: Curatronic storeSource: Curatronic, Curatron Ultra-FlashSource: Curatronic, Curatron Ultra Power 3DApplicator sets vary by device; see the BioReg specification matrix.
    Source: BioReg specification matrix
    Input, measurement or feedbackNo input, measurement, or feedback mechanism is published. The PC software provides a patient data database with treatment follow up, free notes editing, and full report printing including treatment history.Source: Curatronic, Curatron PC SuperCellCom, two dedicated input channels.
    Source: BioReg specification matrix
    PricePublished list pricing with checkout on every clinical model: Curatron PC Bundle $7,250 (listed at $4,850), Premium-Flash Bundle $6,600 (listed at $4,600), Ultra-Flash Bundle $12,865 (listed at $11,300), Ultra Power 3D $13,750.Source: Curatronic store$1,495 to $28,995 across the line. Systems above $5,000 quote financing by inquiry.
    Source: BioReg specification matrix
    WarrantyThree years on the unit, three months on accessories and applicators. Warranty registration must be emailed to the manufacturer within 8 days of delivery to take effect, and warranty shipping costs both ways are the customer's responsibility.Source: Curatronic, privacy and terms2 years device, 1 year accessories, manufacturing defects. Nesta Pro Premium: 5 years device and accessories.
    Source: BioReg specification matrix
    ReturnsUSA and Canada: 30 days from delivery, like-new condition, 20 percent restocking fee. Shipping and customs charges are not refunded and return shipping is the customer's responsibility.Source: Curatronic, privacy and termsSee the BioReg returns policy.
    Source: BioReg specification matrix
    Training includedNo training program is published. Their PC Super page states: “No special training is required for operating this user-friendly PEMF therapy center.”Source: Curatronic, Curatron PC SuperPer device: training video plus 15 minute consult on the home line, onboarding video plus 1 hour live consult on Nesta Pro, white glove training on SanoCenter and CellCom.
    Source: BioReg specification matrix
    Regulatory statusTheir certificates page publishes two images, captioned FDA Listing and a CE certificate. No clearance or approval is claimed on that page.Source: Curatronic, device certificatesFDA registered.
    Source: BioReg specification matrix
    Stated intended userUltra-Flash: “the optimal choice for clinical use.” Premium-Flash: “an excellent solution for practitioners.” PC Super: “a unique solution for a Comprehensive Clinical Therapy Center.” Ultra Power 3D: “designed for clinical applications.”Source: Curatronic, Curatron Ultra-FlashSource: Curatronic, Curatron Premium-FlashSource: Curatronic, Curatron PC SuperSource: Curatronic, Curatron Ultra Power 3DLicensed practitioners and home users.
    Source: BioReg specification matrix

    Curatron publishes intensity per applicator and per model where BioReg publishes a single figure across the line. Curatron’s intensity page.

    Where Curatron publishes more than BioReg

    On disclosure, Curatron is ahead of us, and we would rather say so than leave a buyer to discover it. Curatron publishes per-model specification blocks covering intensity, waveform, pulse rate, program count and duration, dimensions, weight, input voltage and warranty. They publish a pulse rise time of 140 micro seconds. They publish the full selectable parameter set a user can build a protocol from, and offer the complete protocol list as a download. They publish open list pricing with checkout on every clinical model, accessories included. They disclose a side effect of their impulse line in their own material.

    BioReg publishes a single intensity figure across the line, no rise time, program counts without the underlying selectable parameters, and quotes financing by inquiry above $5,000. That is less published detail than Curatron provides, and closing that gap is our work, not a point against them.

    Source: Curatronic, Curatron Ultra-Flash

    Where BioReg publishes more than Curatron

    Curatron publishes no input, measurement, or feedback mechanism of any kind across the clinical line. What their software provides is record keeping: patient demographic data, treatment follow-up notes, and printable treatment history. That is documentation, not measurement. The only field verification method they publish is manual: holding a static magnet above the applicator to detect that a field is present.

    The BioReg CellCom uses two dedicated input channels that read the user during a session and adjust output frequency in response. That is a closed-loop system.

    The BioReg Nesta line is open-loop and performs no physiological measurement.

    Source: Curatronic, Intensity of Curatron PEMF

    What does the published evidence say?

    The BioReg research library holds 50 peer-reviewed studies, each graded on an A through F scale for design and sample quality, organized by condition with citations. Browse the research library or read how studies are graded. This page does not characterize Curatron’s evidence base; their own site describes their research position.

    Which should you consider?

    Based on published positioning, the Curatron clinical line suits a practice that wants a choice between oscillating and impulse output, high published field maxima, open pricing it can budget against without a call, and a software protocol database it can inspect before buying.

    The BioReg line suits a practice that wants low-intensity output across a tiered lineup, included training and onboarding at every level, a multi-station clinic platform, and a closed-loop flagship that measures during the session.

    Neither company’s published material supports a clinical superiority claim in either direction, and this page makes none. On the underlying technical question, Curatron’s own answer stands: it remains an open question.