FDA Cleared 2018-01-23T15:07:41+00:00

Teeter Decompression Devices are

Teeter Decompression Devices have been listed with the FDA as Class 1 medical devices for decades. A 2016 review of new information and studies resulted in FDA clearance for an expanded list of back pain conditions for which the Teeter is indicated and broadened the classification to a range of Teeter decompression devices.

To review the documentation, click here.

Indicated for Back Pain Relief
and common causes:

  • Sciatica
  • Muscle tension
  • Spinal stenosis
  • Spinal degenerative joint disease
  • Herniated discs
  • Facet syndrome
  • Spinal curvature due to tight muscles
  • Degenerative disc disease
  • Muscle spasm


  • DEX II


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