Wonder Touch

GUDID D650WONDER1

XOD Inc.

Medium-wave diathermy treatment system

• Primary Device ID: D650WONDER1
• NIH Device Record Key: e0bb13ea-9d33-4a61-8857-1c899af3f51f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wonder Touch
• Version Model Number: WONDER00001
• Company DUNS: 119238609
• Company Name: XOD Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D650WONDER1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242175

FDA Product Code

• PBX: Massager, Vacuum, Radio Frequency Induced Heat

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: 2025-07-09
• Device Publish Date: 2025-07-01

Devices Manufactured by XOD Inc.

• D650WONDER1 - Wonder Touch: 2025-07-09
• D650WONDER1 - Wonder Touch: 2025-07-09
• G650BREEZE1 - XOD Breeze dermabrasion brush: 2024-07-18
• G650DIOGO1 - XOD DioGo compact diode laser: 2024-07-18