HQNClass II

Conformer, Ophthalmic

21 CFR 886.3130 / Ophthalmic

HQN is the FDA product code for Conformer, Ophthalmic, a class II device type, regulated under 21 CFR 886.3130. As of 2026-09-10, FDA records hold 7 510(k) clearances under this code, the most recent dated 1998-01-20, and one recall.

Classification record

Product code: HQN
Device name: Conformer, Ophthalmic
Regulation: 21 CFR 886.3130
Device class: Class II
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: 7
Ingested recalls: 1

Clearances, product code HQN

By decision year

7 clearances under product code HQN with a decision year between 1977 and 1998, 1992 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code HQN by decision year
Year	Clearances
1977	1
1992	2
1995	1
1997	2
1998	1

Applicants with the most clearances

Product code HQN

Applicants holding the most 510(k) clearances under product code HQN
Applicant	Clearances
Storz Instrument Co.	2
Kolberg Ocular Products, Inc.	1
Porex Surgical, Inc.	1
Robert B. Scott Ocularists of Florida, Inc.	1
Southwest Artificial Eyes, Inc.	1
Xavier A. Guerra, Ocularist, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 28 companies shown, in name order