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SS17K-M

by Micron Corp.

SS17K-M is a Class II device made by Micron Corp., listed in FDA GUDID since 22 Dec 2022 (UDI-DI 04560205914091), 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 Number04560205914091 UDI-DI Date22 Dec 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  • Withdrawn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
SS17K
Generic name
Pneumatic dental scaling/debridement system
Model / reference
SS17K-M
Primary DI / UDI-DI
04560205914091
FDA product code
ELC
GMDN term
Pneumatic dental scaling/debridement system
Device class
Class II
Regulation number
872.4850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code ELC (Scaler, Ultrasonic).

Other devices from Micron Corp.

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)