Skip to content

Ophthalmic Knife K20-2294

by Katena Products, Inc.

Ophthalmic Knife K20-2294 is a Class I device made by Katena Products, Inc., listed in FDA GUDID since 14 Sep 2020 (UDI-DI 00841668113264), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841668113264 UDI-DI Date14 Sep 2020ListedStatusListed 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  • Withdrawn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
Ophthalmic Knife
Generic name
Ophthalmic knife, single-use
Model / Ref / Catalog
K20-2294
Primary DI / UDI-DI
00841668113264
FDA product code
HNN
GMDN term
Ophthalmic knife, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

Related devices

Category: Ophthalmic knife, single-use

Other devices from Katena Products, Inc.

See all devices from Katena Products, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
Other properties (10, all answered No)