gudid
Primary ID: RecoveryTherm Hot/Cold/Vibration Knee
Therabody (UDI RecoveryTherm Hot/Cold/Vibration Knee)
Manufactured by Therabody, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Therabody - Primary ID RecoveryTherm Hot/Cold/Vibration Knee
Device Regulatory Overview
The Therabody (Model/Catalog Number: RecoveryTherm Hot/Cold/Vibration Knee) 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
- RecoveryTherm Hot/Cold/Vibration Knee
- 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 Therabody?
The registered manufacturer of record for Therabody is Therabody, Inc..
What is the Primary UDI-DI identifier for Therabody?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RecoveryTherm Hot/Cold/Vibration Knee.
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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