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AuroSleek C25222HT

by Aurolab

AuroSleek C25222HT is a Class I device made by Aurolab, listed in FDA GUDID since 15 Jun 2023 (UDI-DI 10803878044667), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10803878044667 UDI-DI Date15 Jun 2023ListedStatusListed GUDID: not 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  • Withdrawn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
AuroSleek
Generic name
Ophthalmic knife, single-use
Model / reference
C25222HT
Primary DI / UDI-DI
10803878044667
FDA product code
HNN
GMDN term
Ophthalmic knife, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code HNN (Knife, Ophthalmic).

Other devices from Aurolab

See all devices from Aurolab →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)