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Anodyne Surgical KA2286

by Psi/Eye-Ko, Inc.

Anodyne Surgical KA2286 is a Class I device made by Psi/Eye-Ko, Inc., listed in FDA GUDID since 28 Jul 2023 (UDI-DI 00840516141602), 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 Number00840516141602 UDI-DI Date28 Jul 2023ListedStatusListed 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  • Withdrawn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
Anodyne Surgical
Generic name
Ophthalmic knife, reusable
Model / reference
KA2286
Primary DI / UDI-DI
00840516141602
FDA product code
HNN
GMDN term
Ophthalmic knife, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic knife, reusable

Other devices from Psi/Eye-Ko, Inc.

See all devices from Psi/Eye-Ko, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)