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Johnson-Promident K25L

by Young Innovations, Inc.

Johnson-Promident K25L is a Class I device made by Young Innovations, Inc., listed in FDA GUDID since 24 Nov 2022 (UDI-DI 00843471115022), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00843471115022 UDI-DI Date24 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Johnson-Promident
Generic name
Dental ultrasonic surgical system handpiece
Model / Ref / Catalog
K25L
Primary DI / UDI-DI
00843471115022
FDA product code
EFB
GMDN term
Dental ultrasonic surgical system handpiece
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental ultrasonic surgical system handpiece

Other devices from Young Innovations, Inc.

See all devices from Young Innovations, Inc. →

Properties

  • Sterilise before use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)