Dream TAP (UDI 5200109)
Manufactured by FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC
Device Regulatory Overview
The Dream TAP (Model/Catalog Number: 5200109) is a medical device manufactured by FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5200109
- Product Code / EMDN
- LRK
- Device Name
- Database Sync Date
- 2026-08-09 09:03:40
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 Dream TAP?
The registered manufacturer of record for Dream TAP is FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC.
What is the Primary UDI-DI identifier for Dream TAP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5200109.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC
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