Fascia Buddy Square Cupping Set – 20 pieces CP700

GUDID 00754028870007

The Fascia Buddy Square (FB2) Cups introduce a groundbreaking way to engage myofascial tissues, whether you’re a professional or using them at home. Unlike traditional round cups, which have been used for centuries, FB2 cups come in five different square sizes, allowing for a more effective and continuous decompression experience. Traditional round cups create individual suction zones, but when placed side by side, they leave gaps between them. This results in an uneven decompression area. With FB2 square cups, you can build a seamless decompression zone over muscles and tissues for better results. What Makes FB2 Square Cups Different? FB2 square cups provide a unique advantage—they fit together perfectly to create a continuous decompression zone over the target area. Whether you’re addressing pain, trigger points, or specific muscle shapes, you can select the appropriate size cup and build a customized myofascial decompression matrix. Each FB2 set includes 20 cups in five different sizes, allowing you to create a personalized treatment plan. Need even more coverage? The FB2 Expansion Sets let you build larger and more advanced decompression matrices, giving you limitless possibilities!

Eastern Currents Distributing Ltd

Cupping therapy device

• Primary Device ID: 00754028870007
• NIH Device Record Key: ebf7d759-c3d2-4d4a-b321-c695d3d1092c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fascia Buddy Square Cupping Set – 20 pieces
• Version Model Number: CP700
• Catalog Number: CP700
• Company DUNS: 257053454
• Company Name: Eastern Currents Distributing Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00754028870007 [Primary]

FDA Product Code

• LYG: Massager, Therapeutic, Manual

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-25
• Device Publish Date: 2025-08-15

Devices Manufactured by Eastern Currents Distributing Ltd

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