FDA Registered2018-05-17T08:34:38+00:00

Teeter Decompression Devices are
FDA REGISTERED

Teeter Decompression Devices are registered with the FDA as 510(k) medical devices, designed to provide traction to the spine while stretching the para-spinal muscles. Teeter is the ONLY brand that is both UL safety certified and 510(k) registered with the FDA as a class one medical device. That makes Teeter THE name to trust.

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

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