pma
Primary ID: P040013
GEM 21S GROWTH FACTOR ENCHANCED MATRIX (UDI P040013)
Manufactured by Lynch Biologics, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GEM 21S GROWTH FACTOR ENCHANCED MATRIX - Primary ID P040013
Device Regulatory Overview
The GEM 21S GROWTH FACTOR ENCHANCED MATRIX (Model/Catalog Number: Unspecified) is a medical device manufactured by Lynch Biologics, LLC. This product is indexed under FDA Product Code / Category Classification NPZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- NPZ
- Device Name
- Bone grafting material, dental, with biologic component
- Database Sync Date
- 2026-08-09 10:06:14
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 GEM 21S GROWTH FACTOR ENCHANCED MATRIX?
The registered manufacturer of record for GEM 21S GROWTH FACTOR ENCHANCED MATRIX is Lynch Biologics, LLC.
What is the Primary UDI-DI identifier for GEM 21S GROWTH FACTOR ENCHANCED MATRIX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P040013.
What classification code is assigned to this device?
This device is registered under product classification code NPZ.
Similar Classification Devices (NPZ)
Other Devices by Lynch Biologics, LLC
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