HQDClass II

Lens, Contact (Other Material) - Daily

21 CFR 886.5916 / Ophthalmic

HQD is the FDA product code for Lens, Contact (Other Material) - Daily, a class II device type, regulated under 21 CFR 886.5916. As of 2026-09-10, FDA records hold 118 510(k) clearances under this code, the most recent dated 2026-03-27, and 5 recalls.

Classification record

Product code: HQD
Device name: Lens, Contact (Other Material) - Daily
Regulation: 21 CFR 886.5916
Device class: Class II
Review panel: Ophthalmic
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 118
Ingested recalls: 5

Clearances, product code HQD

By decision year

118 clearances under product code HQD with a decision year between 1984 and 2026, 2000 the highest year at 10.

Show the numbers

510(k) clearances under FDA product code HQD by decision year
Year	Clearances
1984	2
1994	7
1995	2
1996	8
1997	4
1998	3
1999	5
2000	10
2001	4
2002	7
2003	1
2004	2
2005	3
2006	5
2007	4
2008	5
2009	2
2011	2
2012	2
2014	1
2016	7
2017	9
2018	5
2019	2
2020	1
2021	3
2022	3
2023	3
2024	5
2026	1

Applicants with the most clearances

Product code HQD

Applicants holding the most 510(k) clearances under product code HQD
Applicant	Clearances
Acuity Polymers Inc.	11
Contamac Ltd.	11
Paragon Vision Sciences, Inc.	11
Synergeyes, Inc.	11
Polymer Technology Corp.	8
Bausch & Lomb Incorporated	7
Menicon Co. Ltd.	5
Innovision, Inc.	3
The Lagado Corp.	3
Valley Contax, Inc	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order