Bite fork

FDA UDI

Class I (US FDA UDI)

by Candulor AG

Identity

Trade Name: Bite fork FDA UDI
Generic Name: Dental articulator FDA UDI
Device Name: Bite fork FDA UDI
Model / Reference: 662451 FDA UDI
Description: Bite fork FDA UDI

Identifiers

Catalog Number: 662451 FDA UDI
Primary DI / UDI-DI: E1996624511 FDA UDI
FDA Product Code: KCR FDA UDI
GMDN Term: Dental articulator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3220 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental articulator

Bite fork by Candulor AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MA2340 W/STRAPS — WHIP-MIX CORP. · Class I
Hanau Wide-Vue Articulator — WHIP-MIX CORP. · Class I
2240 Q Articulator — WHIP-MIX CORP. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Candulor AG

Sources (1)

FDA UDI fe1fce5c-c6fa-4098-9334-750a028d8b08 34 fields · synced May 30, 2026