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Dmg 220600

by DMG America LLC

Dmg 220600 is a Class I device made by DMG America LLC, listed in FDA GUDID since 6 Nov 2025 (UDI-DI 00325047000005), 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 Number00325047000005 UDI-DI Date6 Nov 2025ListedStatusListed 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  • Withdrawn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
Dmg
Generic name
Dental material cartridge-plunging applicator, single-component
Model / Ref / Catalog
220600
Primary DI / UDI-DI
00325047000005
FDA product code
EID
GMDN term
Dental material cartridge-plunging applicator, single-component
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Other devices from DMG America LLC

See all devices from DMG America LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)