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Secure-Lock 102-1377

by Xiros Ltd

Secure-Lock 102-1377 is a Class II device made by Xiros Ltd, listed in FDA GUDID since 27 Jul 2022 (UDI-DI 05060267132000), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060267132000 UDI-DI Date27 Jul 2022ListedStatusListed GUDID: not 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  • Withdrawn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
Secure-Lock
Generic name
Tendon/ligament bone anchor, non-bioabsorbable
Model / reference
102-1377
Primary DI / UDI-DI
05060267132000
FDA product code
GAT, HTY
GMDN term
Tendon/ligament bone anchor, non-bioabsorbable
Device class
Class II
Regulation number
878.5000, 888.3040
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene).

Other devices from Xiros Ltd

See all devices from Xiros Ltd →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)