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Ophthalmic Scissors K4-3100

by Katena Products, Inc.

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

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 Number00841668105320 UDI-DI Date14 Sep 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ophthalmic Scissors
Generic Name
Intraocular scissors, conventional-hinge, reusable
Model / Ref / Catalog
K4-3100
Primary DI / UDI-DI
00841668105320
FDA Product Code
HNF
GMDN Term
Intraocular scissors, conventional-hinge, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution

Other devices from Katena Products, Inc.

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Properties

  • Prescription Use
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No