Coffret DENTOCLIC Fibre de verre

FDA UDI

Class I (US FDA UDI)

by Itena Clinical

Identity

Trade Name: Coffret DENTOCLIC Fibre de verre FDA UDI
Generic Name: Dental restoration retention pin kit FDA UDI
Model / Reference: Coffret translucide FDA UDI

Identifiers

Catalog Number: KFVT20 FDA UDI
Primary DI / UDI-DI: 03760260225014 FDA UDI
FDA Product Code: ELR FDA UDI
GMDN Term: Dental restoration retention pin kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental restoration retention pin kit

Coffret DENTOCLIC Fibre de verre by Itena Clinical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration retention pin kit.

Preat — PREAT Corporation · Class I
Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
Coffret DENTOCLIC Fibre de verre — ITENA CLINICAL · 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: Itena Clinical

Sources (1)

FDA UDI aa35a944-4171-43af-abb8-23385553491d 33 fields · synced Jun 1, 2026