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NewFlora | Pelvic & Perineal Massage Wand
  • NewFlora | Pelvic & Perineal Massage Wand
  • NewFlora | Pelvic & Perineal Massage Wand
  • NewFlora | Pelvic & Perineal Massage Wand
NewFlora | Pelvic & Perineal Massage Wand

NewFlora | Pelvic & Perineal Massage Wand

$29.99

What is this product?
A dual-ended massage wand for perineal massage and pelvic wellness, designed by a Doctor of Physical Therapy.

Key features and benefits:
Versatile design for rectal or vaginal use, helping you customize your self-care and support pelvic health.

What else you need to know:
Created by a pelvic health expert to put you in control of your wellness routine—your body, your rules.

Learn more about Pelvic Wands here!

This Product is: BPA Free, Latex Free, Non-Toxic, Paraben Free

How to Use & Care Instructions

How to Use

  1. Wash with warm water and soap between each use.
  2. Either end can be used, chose what is more comfortable for you.
  3. Generously apply water-based lubricant to the wand and vagina.
  4. Lie on your back with bent knees.
  5. Breathe deeply in and out, insert on the exhale.
  6. Think of the vagina as a clock, 9 o'clock is the right side and 3 o'clock is the left side of the vagina. Sweep from 5 to 1 o'clock and 7 to 11 o'clock
  7. Repeat 1 -2x/ day, using different depths of insertion as needed.
Ingredients & Materials

Ultra-Smooth Medical Grade Silicone
Return Policy & Shipping Costs

Return Policy: Returns must be initiated within 14 days. Items must be undamaged, unworn, unused, and have tags attached. Claims for damaged or defective products must be made within 5 days of receipt.

Shipping Cost (U.S.): Free Shipping

Ladibug offers free shipping for carts with a value over $50!

About the Brand

NewFlora is a brand known for focusing on women's health and wellness, offering a variety of products aimed at promoting pelvic health and overall well-being.

Shop All NewFlora Products here!

Product Highlights

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This Product is: FDA Cleared

What does it mean? "FDA cleared" means that the FDA has reviewed a medical device through the 510(k) premarket notification process and determined it to be substantially equivalent in safety and effectiveness to a legally marketed device, allowing it to be sold in the U.S. This clearance signifies that the device can be marketed, but it does not imply FDA approval or endorsement.

Learn more about Ladibug Stamps here!

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