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gSource gS 87.0020

by Gsource, LLC.

gSource gS 87.0020 is a Class I device made by Gsource, LLC., listed in FDA GUDID since 3 Mar 2020 (UDI-DI 00840314247032), 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 Number00840314247032 UDI-DI Date3 Mar 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  • Withdrawn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
Orthopaedic ball spike
Model / Ref / Catalog
gS 87.0020
Primary DI / UDI-DI
00840314247032
FDA product code
LXH
GMDN term
Orthopaedic ball spike
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic ball spike

Similar devices

Other devices filed under FDA product code LXH (Orthopedic Manual Surgical Instrument).

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)