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Johnson-Promident

FDA UDI

Class II (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Johnson-Promident FDA UDI
Generic Name
Dental abrasive air jet system handpiece FDA UDI
Device Name
MINIBLASTER MALE QUICK DISCONNECT FDA UDI
Model / Reference
505128 FDA UDI
Description
MINIBLASTER MALE QUICK DISCONNECT FDA UDI

Identifiers

Catalog Number
505128 FDA UDI
Primary DI / UDI-DI
00840326418499 FDA UDI
510(k) Number
K013969 FDA UDI
FDA Product Code
KOJ FDA UDI
GMDN Term
Dental abrasive air jet system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6080 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental abrasive air jet system handpiece

Johnson-Promident by Young Innovations, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive air jet system handpiece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af2bf956-7cb2-40d4-bf0e-b85930847214 36 fields · synced May 30, 2026