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Vanguard XP® Instrumentation 32-700337

by Biomet Orthopedics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

12 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 Number00887868500978 UDI-DI Date2 Apr 2021ListedStatusListed GUDID: in commercial distribution

Recalls

12 recalls · FDA

  • 12 recalls, same reason

    • Terminated Z-2530-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2503-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2515-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2537-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2533-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2528-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2532-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2535-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2536-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2531-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2529-2019 FDA Class II initiated 15 Aug 2019
    • Terminated Z-2534-2019 FDA Class II initiated 15 Aug 2019

    The locking bar not fully engaging

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Vanguard XP® Instrumentation
Generic name
Surgical implant template, reusable
Model / Ref / Catalog
32-700337
Primary DI / UDI-DI
00887868500978
510(k) Number
FDA product code
OIY, JWH, MBV, MBH
GMDN term
Surgical implant template, reusable
Device class
Class II
Regulation number
888.3560, 888.3565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical implant template, reusable

Cleared under the same submission (K122160)

Show all (12)

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number

Other properties (12)

  • Supplied sterile: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No