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Luxator LK VET

by Directa AB 2 variants

Luxator LK VET (506332U) is a Class I device made by Directa AB, listed in FDA GUDID since 19 Feb 2025 (UDI-DI 17310230021646), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number17310230021646 UDI-DI Date19 Feb 2025ListedStatusListed GUDID: 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  • Withdrawn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
Luxator
Generic name
Periotome, reusable
Model / Ref / Catalog
LK VET, 506332U
Description
17310231050485 17310231050461 17310231050430 17310231050416 17310231050454
Primary DI / UDI-DI
17310230021646
FDA product code
EMJ
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periotome, reusable

Other devices from Directa AB

See all devices from Directa AB →

Properties

  • Sterilise before use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)