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Young

FDA UDI

Class I (US FDA UDI)

by Young Dental Manufacturing I, Llc

Identity

Trade Name
Young FDA UDI
Generic Name
Pneumatic dental scaling/debridement system handpiece FDA UDI
Device Name
Young Cordless Handpiece System, White FDA UDI
Model / Reference
295721 FDA UDI
Description
Young Cordless Handpiece System, White FDA UDI

Identifiers

Catalog Number
295721 FDA UDI
Primary DI / UDI-DI
00302732957219 FDA UDI
510(k) Number
K171377 FDA UDI
FDA Product Code
EKX FDA UDI
GMDN Term
Pneumatic dental scaling/debridement system handpiece 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Pneumatic dental scaling/debridement system handpiece

Young by Young Dental Manufacturing I, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic dental scaling/debridement system handpiece.

Cleared under the same submission

K171377 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Young Dental Manufacturing I, Llc

Sources (1)

  • FDA UDI 109a6ff5-b579-4105-af83-106f2c4cb7fb 36 fields · synced May 30, 2026