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Johnson-Promident

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Johnson-Promident FDA UDI
Generic Name
Dental ultrasonic surgical system handpiece FDA UDI
Device Name
FIBER OPTIC 1:5 CONTRA ANGLE FOR KAVO (25LPA/LHA) W/ INTERNAL WATER) FDA UDI
Model / Reference
K25L FDA UDI
Description
FIBER OPTIC 1:5 CONTRA ANGLE FOR KAVO (25LPA/LHA) W/ INTERNAL WATER) FDA UDI

Identifiers

Catalog Number
K25L FDA UDI
Primary DI / UDI-DI
00843471115022 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental ultrasonic surgical 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

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 ultrasonic surgical system handpiece

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

Similar devices

Also classified as Dental ultrasonic surgical system handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d7a54d1e-913c-481d-898e-cf43a51fb0ec 35 fields · synced Jun 8, 2026