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Dexcom G6 Android SW11678

by Dexcom

Dexcom G6 Android SW11678 is a Class II device made by Dexcom, listed in FDA GUDID since 25 Apr 2018 (UDI-DI 00386270000811), 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 Number00386270000811 UDI-DI Date25 Apr 2018ListedStatusListed 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  • Withdrawn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
Dexcom G6 Android
Generic name
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Model / reference
SW11678
Primary DI / UDI-DI
00386270000811
FDA product code
QBJ
GMDN term
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Device class
Class II
Regulation number
862.1355
GUDID distribution status
In Commercial Distribution

Related devices

Category: Percutaneous interstitial fluid glucose monitoring system, electrochemical

Other devices from Dexcom

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Properties

Other properties (15, all answered No)