HNFClass I

Scissors, Ophthalmic

21 CFR 886.4350 / Ophthalmic

HNF is the FDA product code for Scissors, Ophthalmic, a class I device type, regulated under 21 CFR 886.4350. As of 2026-09-10, FDA records hold 15 510(k) clearances under this code, the most recent dated 2002-11-01, and 2 recalls.

Classification record

Product code: HNF
Device name: Scissors, Ophthalmic
Regulation: 21 CFR 886.4350
Device class: Class I
Review panel: Ophthalmic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 15
Ingested recalls: 2

Clearances, product code HNF

By decision year

15 clearances under product code HNF with a decision year between 1976 and 2002, 1976 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code HNF by decision year
Year	Clearances
1976	4
1977	3
1981	1
1982	3
1985	1
1987	1
1990	1
2002	1

Applicants with the most clearances

Product code HNF

Applicants holding the most 510(k) clearances under product code HNF
Applicant	Clearances
J. Sklar Mfg. Co., Inc.	3
V. Mueller O.V. Baxter Healthcare Corp.	3
Conphar, Inc.	2
Alcon Laboratories	1
Artiberia	1
Depuy, Inc.	1
Keeler Instruments, Inc.	1
Microline Pentax, Inc.	1
Robert I. Chien & Assoc., Inc.	1
Stephens Instruments, Inc	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 250 companies shown, in name order