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AG Neovo

FDA UDI

Class I (US FDA UDI)

by Associated Industries China, Inc.

Identity

Trade Name
AG Neovo FDA UDI
Generic Name
Dental power tool system handpiece, pneumatic FDA UDI
Device Name
Dental Low-speed Handpieces and Accessories FDA UDI
Model / Reference
REVOLUTION R-2005 FDA UDI
Description
Dental Low-speed Handpieces and Accessories FDA UDI

Identifiers

Primary DI / UDI-DI
04710739590265 FDA UDI
FDA Product Code
EFB FDA UDI
EGS FDA UDI
GMDN Term
Dental power tool system handpiece, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool system handpiece, pneumaticDental power tool system, line-powered

AG Neovo by Associated Industries China, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool system, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Associated Industries China, Inc.

Sources (1)

  • FDA UDI 9f12f051-f01b-46a1-8d66-4c677cb300a1 33 fields · synced May 30, 2026