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MANI PLUGGERS 21mm #40

by Mani, Inc.

MANI PLUGGERS 21mm #40 is a Class I device made by Mani, Inc., listed in FDA GUDID since 8 Oct 2022 (UDI-DI 04546951506179), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04546951506179 UDI-DI Date8 Oct 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  • Withdrawn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
Mani Pluggers
Generic name
Endodontic plugger
Model / reference
21mm #40
Primary DI / UDI-DI
04546951506179
FDA product code
EKR
GMDN term
Endodontic plugger
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endodontic plugger

Other devices from Mani, Inc.

See all devices from Mani, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)