gudid
Primary ID: Wave Solo
Theragun (UDI Wave Solo)
Manufactured by Therabody, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Theragun - Primary ID Wave Solo
Device Regulatory Overview
The Theragun (Model/Catalog Number: Wave Solo) is a medical device manufactured by Therabody, Inc.. This product is indexed under FDA Product Code / Category Classification ISA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Wave Solo
- Product Code / EMDN
- ISA
- Device Name
- Database Sync Date
- 2026-08-09 09:17:03
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Theragun?
The registered manufacturer of record for Theragun is Therabody, Inc..
What is the Primary UDI-DI identifier for Theragun?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Wave Solo.
What classification code is assigned to this device?
This device is registered under product classification code ISA.
Similar Classification Devices (ISA)
Other Devices by Therabody, Inc.
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