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smarThor G03

by Dmetec.Co., Ltd.

smarThor G03 is a dental ultrasonic surgical system (FDA Class II; FDA product code DZI, Drill, Bone, Powered) made by Dmetec.Co., Ltd., listed in FDA GUDID since 31 Jan 2017 (UDI-DI 08809462190029), 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 Number08809462190029 UDI-DI Date31 Jan 2017ListedStatusListed 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  • Withdrawn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
smarThor
Generic name
Dental ultrasonic surgical system
Model / reference
G03
Primary DI / UDI-DI
08809462190029
FDA product code
DZI
GMDN term
Dental ultrasonic surgical system
Device class
Class II
Regulation number
872.4120
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental ultrasonic surgical system

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See all devices from Dmetec.Co., Ltd. →

Properties

  • Sterilise before use
  • Serial number
Other properties (13, all answered No)