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Marking Pin 98520-2229

by Captiva Spine

Marking Pin 98520-2229 is a Class I device made by Captiva Spine, listed in FDA GUDID since 28 Oct 2026 (UDI-DI M739985202229), 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 NumberM739985202229 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  • Withdrawn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
Marking Pin
Generic name
Orthopaedic prosthesis implantation positioning instrument, single-use
Model / reference
98520-2229
Primary DI / UDI-DI
M739985202229
FDA product code
LXH, KIL, FZX
GMDN term
Orthopaedic prosthesis implantation positioning instrument, single-use
Device class
Class I
Regulation number
888.4540, 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
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)