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Corning 6929

by Corning Incorporated

Corning 6929 is a Class I device made by Corning Incorporated, listed in FDA GUDID since 19 May 2022 (UDI-DI H10869293), 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 NumberH10869293 UDI-DI Date19 May 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Corning
Generic name
Blood centrifugation system containment kit
Model / Ref / Catalog
6929
Primary DI / UDI-DI
H10869293
FDA product code
LXG
GMDN term
Blood centrifugation system containment kit
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood centrifugation system containment kit

Similar devices

Other devices filed under FDA product code LXG (EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE).

Other devices from Corning Incorporated

See all devices from Corning Incorporated →

Properties

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