gudid
Primary ID: REX TL 2.9 H15
PiezoImplant System (UDI REX TL 2.9 H15)
Manufactured by Rex Implants, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PiezoImplant System - Primary ID REX TL 2.9 H15
Device Regulatory Overview
The PiezoImplant System (Model/Catalog Number: REX TL 2.9 H15) is a medical device manufactured by Rex Implants, Inc.. This product is indexed under FDA Product Code / Category Classification NRQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- REX TL 2.9 H15
- Product Code / EMDN
- NRQ
- Device Name
- REX TL 2.9 H15 Assembly (Implant, Retention Screw TL 2.9, Transfer / Straight Abutment TL 2.9) packaged with Cover Screw TL 2.9
- Database Sync Date
- 2026-08-09 09:03:34
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 PiezoImplant System?
The registered manufacturer of record for PiezoImplant System is Rex Implants, Inc..
What is the Primary UDI-DI identifier for PiezoImplant System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is REX TL 2.9 H15.
What classification code is assigned to this device?
This device is registered under product classification code NRQ.
Similar Classification Devices (NRQ)
Other Devices by Rex Implants, Inc.
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