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Discectomy Prep Tray 25300-1012

by Captiva Spine

Discectomy Prep Tray 25300-1012 is a Class I device made by Captiva Spine, listed in FDA GUDID since 28 Oct 2026 (UDI-DI M739253001012), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM739253001012 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
Discectomy Prep Tray
Generic name
Instrument tray, reusable
Model / reference
25300-1012
Primary DI / UDI-DI
M739253001012
FDA product code
FSM
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Captiva Spine

See all devices from Captiva Spine →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)