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M-Tip L16

by Micron Corp.

M-Tip L16 is a Class I device made by Micron Corp., listed in FDA GUDID since 1 Jul 2023 (UDI-DI 04560205919010), 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 Number04560205919010 UDI-DI Date1 Jul 2023ListedStatusListed 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  • Withdrawn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
M-Tip
Generic name
Pneumatic dental scaling/debridement system handpiece tip, endodontic, reusable
Model / reference
L16
Primary DI / UDI-DI
04560205919010
FDA product code
EKS
GMDN term
Pneumatic dental scaling/debridement system handpiece tip, endodontic, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Pneumatic dental scaling/debridement system handpiece tip, endodontic, reusable

Similar devices

Other devices filed under FDA product code EKS (File, Pulp Canal, Endodontic).

Other devices from Micron Corp.

See all devices from Micron Corp. →

Properties

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