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Hydrolux by 3D Dental

FDA UDI

Class I (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
Hydrolux by 3D Dental FDA UDI
Generic Name
Pneumatic dental power tool system handpiece tip, reusable FDA UDI
Device Name
HYDROLUX PUSH BOTTON HANDPIECE FDA UDI
Model / Reference
HP-PB FDA UDI
Description
HYDROLUX PUSH BOTTON HANDPIECE FDA UDI

Identifiers

Catalog Number
HP-PB FDA UDI
Primary DI / UDI-DI
00817169028024 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Pneumatic dental power tool system handpiece tip, reusable 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pneumatic dental power tool system handpiece tip, reusable

Hydrolux by 3D Dental by 3d Dental Designs And Development, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic dental power tool system handpiece tip, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3d Dental Designs And Development, Llc

Sources (1)

  • FDA UDI 9e7c0ff5-3c02-420b-a856-bffc6d65314d 34 fields · synced May 30, 2026