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Non-Modular Convex Trial 19399-0906

by Captiva Spine

Non-Modular Convex Trial 19399-0906 is a Class I device made by Captiva Spine, listed in FDA GUDID since 28 Oct 2026 (UDI-DI M739193990906), 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 NumberM739193990906 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  • Withdrawn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
Non-Modular Convex Trial
Generic name
General internal orthopaedic fixation system implantation kit
Model / reference
19399-0906
Primary DI / UDI-DI
M739193990906
FDA product code
LXH
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
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
Other properties (12, all answered No)