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FDA Clears DyAnsys Neurostimulation Device Primary Relief to Treat C-Section Pain


News provided by

DyAnsys Inc.

Jul 28, 2022, 09:30 ET

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PALO ALTO, Calif., July 28, 2022 /PRNewswire/ -- DyAnsys, Inc., has announced that Primary Relief, a percutaneous electrical neurostimulation device, has been clearedto treat pain following a Caesarean-section (C-section).

The percutaneous electrical nerve stimulator (PENS) system can be used for up to three days for symptomatic relief of post-operative pain following a C-section delivery.

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Primary Relief, a PENS device, is a significant alternative to opioids for the treatment of pain following a C-section.

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Demonstrating testing for placement of Primary Relief, a percutaneous electrical neurostimulation device cleared for treating pain following a Cesarean section (C-section). The device is manufactured and distributed by DyAnsys Inc.
Demonstrating testing for placement of Primary Relief, a percutaneous electrical neurostimulation device cleared for treating pain following a Cesarean section (C-section). The device is manufactured and distributed by DyAnsys Inc.

"This device has been shown to make a difference for patients, effectively relieving pain without reliance on opioids or other analgesics. This is a significant advancement in providing options to women," said DyAnsys Chief Executive Srini Nageshwar. "We look forward to connecting with physicians and hospitals to providing this alternative to their patients."

The wearable, battery-operated device is designed to administer periodic low level electrical pulses to the ear over 72 hours from the activation of the device. The electrical pulses are delivered to branches of the cranial nerves on the ear through a wire assembly and stimulation needles.

The effectiveness of the device was demonstrated in a single-center, double arm, randomized, controlled, parallel assignment prospective study involving 44 participants who underwent C-section delivery. The analysis showed that minimally invasive nerve stimulation intervention using Primary Relief device reduced the pain score faster than the standard analgesics. No additional opioid analgesics were required. No complications or adverse events were observed in any of the participants during the study period.

The nonclinical testing of Primary Relief device included biocompatibility testing, electrical safety (electromagnetic compatibility and safety), performance bench testing and software verification and validation.

DyAnsys offers two companion PENS devices - First Relief, with FDA clearance for the treatment of diabetic neuropathic pain, and Drug Relief, with FDA clearance as an aid to drug withdrawal.

DyAnsys Inc. is a global company headquartered in California with subsidiaries in Switzerland and India. DyAnsys provides advanced medical diagnostic and monitoring systems to clinicians in individual practices and hospitals. DyAnsys, ANSiscope. First Relief, Primary Relief and Drug Relief are registered trademarks, of DyAnsys, Inc.

Website: www.dyansys.com   

For more information, contact Srini Nageshwar, (888) 950-4321

SOURCE DyAnsys Inc.

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