VividEtch 40% Jumbo 60gm Refill (UDI Z060320)
Manufactured by PEARSON DENTAL SUPPLIES, INC.
Device Regulatory Overview
The VividEtch 40% Jumbo 60gm Refill (Model/Catalog Number: Z060320) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification KLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Z060320
- Product Code / EMDN
- KLE
- Device Name
- Database Sync Date
- 2026-08-09 09:15:03
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of VividEtch 40% Jumbo 60gm Refill?
The registered manufacturer of record for VividEtch 40% Jumbo 60gm Refill is PEARSON DENTAL SUPPLIES, INC..
What is the Primary UDI-DI identifier for VividEtch 40% Jumbo 60gm Refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z060320.
What classification code is assigned to this device?
This device is registered under product classification code KLE.
Similar Classification Devices (KLE)
Other Devices by PEARSON DENTAL SUPPLIES, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint