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gSource gS 27.0000

by Gsource, LLC.

gSource gS 27.0000 is a Class I device made by Gsource, LLC., listed in FDA GUDID since 8 Jan 2020 (UDI-DI 00840314209610), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840314209610 UDI-DI Date8 Jan 2020ListedStatusListed 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  • Withdrawn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
gSource
Generic name
Lens loop, reusable
Model / Ref / Catalog
gS 27.0000
Primary DI / UDI-DI
00840314209610
FDA product code
JYQ
GMDN term
Lens loop, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Lens loop, reusable

Similar devices

Other devices filed under FDA product code JYQ (Loop, Wire).

Other devices from Gsource, LLC.

See all devices from Gsource, LLC. →

Properties

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