Neodent

FDA UDI

Class I (US FDA UDI)

by JJGC Indústria e Comércio de Materiais Dentários S/A.

Identity

Trade Name: Neodent FDA UDI
Generic Name: Surgical drill guide, single-use FDA UDI
Device Name: DRILL GUIDE FOR WS AND CM ZYGOMATIC SCREW REMOVAL FDA UDI
Model / Reference: 103.236 FDA UDI
Description: DRILL GUIDE FOR WS AND CM ZYGOMATIC SCREW REMOVAL FDA UDI

Identifiers

Catalog Number: 103.236 FDA UDI
Primary DI / UDI-DI: 07898237562490 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Surgical drill guide, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical drill guide, single-use

Neodent by JJGC Indústria e Comércio de Materiais Dentários S/A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: JJGC Indústria e Comércio de Materiais Dentários S/A.

Sources (1)

FDA UDI 13f9bda6-f567-4105-84d4-391fa4f4877c 36 fields · synced May 30, 2026