FDA Approved Opioid Detox and Pain Management

The Morph device has demonstrated effectiveness across various types of pain. Its current FDA approvals include:

  • Diabetic Neuropathy
  • Opioid Withdrawal
  • Post-Surgical Pain Management (Cardiovascular and C-Section)
  • Irritable Bowel Syndrome (IBS) in Children

CLICK FOR LINK TO  FULL FDA APPROVAL DOCUMENT

While the Morph Device has very minimal to no side effects there are a few considerations and contraindications:

  • It is a physician prescribed device and is not directly available to the public
  • It is categorized as a Class II medical device and is contraindicated for patients with cardiac pacemakers, hemophilia and psoriasis vulgaris
  • Side effects of the device are generally rare but could include skin irritation, bleeding or infection at the site, pain at the pin site, sore ear, allergic reactions to the tape/adhesive.
  • Avoid driving or operating machinery for the first 24 hours after application, or if dizziness or lightheadedness persists