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Cardioxyl® 73S20Y

by Peters Surgical

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

2 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03661522101391 UDI-DI Date5 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

2 recalls · FDA

  • 2 recalls, same reason

    • Terminated Z-2676-2014 FDA Class II initiated 25 Jun 2014
    • Terminated Z-2675-2014 FDA Class II initiated 25 Jun 2014

    A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Cardioxyl®
Generic Name
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Model / Reference
73S20Y
Primary DI / UDI-DI
03661522101391
510(k) Number
FDA Product Code
GAT
GMDN Term
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Device Class
Class II
Regulation Number
878.5000
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K060163)

Show all (12)

Other devices from Peters Surgical

See all devices from Peters Surgical →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No