Skip to content

Cortera 1506-2940300

by Xtant Medical Holdings, Inc.

Cortera 1506-2940300 is a spinal guidewire (FDA Class I; FDA product code LXH, Orthopedic manual surgical instrument) made by Xtant Medical Holdings, Inc., listed in FDA GUDID since 6 Jan 2023 (UDI-DI 00840311209262), 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 Number00840311209262 UDI-DI Date6 Jan 2023ListedStatusListed 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  • Withdrawn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
Cortera
Generic name
Spinal guidewire
Model / reference
1506-2940300
Primary DI / UDI-DI
00840311209262
FDA product code
LXH
GMDN term
Spinal guidewire
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Spinal guidewire

Similar devices

Other devices filed under FDA product code LXH (Orthopedic manual surgical instrument).

Other devices from Xtant Medical Holdings, Inc.

See all devices from Xtant Medical Holdings, Inc. →

Properties

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