gudid
Primary ID: FORE
FORENDO PASTE (UDI FORE)
Manufactured by PULPDENT CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FORENDO PASTE - Primary ID FORE
Device Regulatory Overview
The FORENDO PASTE (Model/Catalog Number: FORE) is a medical device manufactured by PULPDENT CORPORATION. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FORE
- Product Code / EMDN
- KIF
- Device Name
- CALCIUM HYDROXIDE WITH IODOFORM IN SILICON OIL BASE2.2 gm syringe + 20 applicator tips
- Database Sync Date
- 2026-08-09 09:03:00
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 FORENDO PASTE?
The registered manufacturer of record for FORENDO PASTE is PULPDENT CORPORATION.
What is the Primary UDI-DI identifier for FORENDO PASTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FORE.
What classification code is assigned to this device?
This device is registered under product classification code KIF.
Similar Classification Devices (KIF)
Other Devices by PULPDENT CORPORATION
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