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Impaction T-Handle 98324-0300

by Captiva Spine

Impaction T-Handle 98324-0300 is a Class I device made by Captiva Spine, listed in FDA GUDID since 23 Oct 2026 (UDI-DI M739983240300), 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 NumberM739983240300 UDI-DI Date23 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  • Withdrawn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
Impaction T-Handle
Generic name
Surgical instrument handle, non-torque-limiting
Model / reference
98324-0300
Primary DI / UDI-DI
M739983240300
FDA product code
LXH
GMDN term
Surgical instrument handle, non-torque-limiting
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)