Identity

Trade Name
Neodent FDA UDI
Generic Name
Orthodontic anchoring screw FDA UDI
Device Name
SELF-DRILLING ANCHORAGE IMPLANT MB FDA UDI
Model / Reference
109.487 FDA UDI
Description
SELF-DRILLING ANCHORAGE IMPLANT MB FDA UDI

Identifiers

Catalog Number
109.487 FDA UDI
Primary DI / UDI-DI
07898237567532 FDA UDI
FDA Product Code
OAT FDA UDI
GMDN Term
Orthodontic anchoring screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.3 Millimeter FDA UDI
Length — 7 Millimeter FDA UDI

Category: Orthodontic anchoring screw

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

Similar devices

Also classified as Orthodontic anchoring screw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c71bd6cd-594b-41c7-98e4-ebe08e1b46f9 37 fields · synced Jun 1, 2026