Skip to content

OrthAlign Plus 403168

by Orthalign, Inc.

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

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 Number00858704006688 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
OrthAlign Plus
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
403168
Primary DI / UDI-DI
00858704006688
FDA product code
OLO
GMDN term
Orthopaedic surgical procedure kit, non-medicated, reusable
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Other devices from Orthalign, Inc.

  • Lantern ASC 503000

    Class II

  • Lantern ASC 407001-02

    Class II

  • Lantern 405310 Open recall

    Class II

  • Lantern ASC 407001-01

    Class II

  • Lantern 402546 Open recall

    Class II

  • Lantern ASC 407000

    Class II

See all devices from Orthalign, 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