gudid
Primary ID: 0151
LISA APPLIANCE (UDI 0151)
Manufactured by Ortho Solutions, LC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LISA APPLIANCE - Primary ID 0151
Device Regulatory Overview
The LISA APPLIANCE (Model/Catalog Number: 0151) is a medical device manufactured by Ortho Solutions, LC. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0151
- Product Code / EMDN
- LRK
- Device Name
- LISA ORAL SLEEP APNEA APPLIANCE
- Database Sync Date
- 2026-08-09 09:03:36
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 LISA APPLIANCE?
The registered manufacturer of record for LISA APPLIANCE is Ortho Solutions, LC.
What is the Primary UDI-DI identifier for LISA APPLIANCE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0151.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Ortho Solutions, LC
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