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Lantern 502000-03-US

by Orthalign, Inc.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K262253

FDA submission, from GUDID

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 Number00810832032502 UDI-DI Date24 Aug 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK262253 Date31 Jul 2026DecidedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Lantern
Generic name
Orthopaedic stereotactic surgery system
Model / Ref / Catalog
502000-03-US
Primary DI / UDI-DI
00810832032502
510(k) Number
FDA product code
ONN
GMDN term
Orthopaedic stereotactic surgery system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

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

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date

Other properties (9)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Manufacturing date: No