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gSource gS 46.1655

by Gsource, LLC.

gSource gS 46.1655 is a Class I device made by Gsource, LLC., listed in FDA GUDID since 3 Jan 2020 (UDI-DI 00840314222312), 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 Number00840314222312 UDI-DI Date3 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  • Withdrawn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
Bone holding forceps
Model / Ref / Catalog
gS 46.1655
Primary DI / UDI-DI
00840314222312
FDA product code
GEN
GMDN term
Bone holding forceps
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone holding forceps

Similar devices in this category

Other devices filed under Bone holding forceps.

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)