HQGClass I

Lens, Spectacle, Non-Custom (Prescription)

21 CFR 886.5844 / Ophthalmic

HQG is the FDA product code for Lens, Spectacle, Non-Custom (Prescription), a class I device type, regulated under 21 CFR 886.5844. As of 2026-09-10, FDA records hold 56 510(k) clearances under this code, the most recent dated 1994-02-16, and 4 recalls.

Classification record

Product code: HQG
Device name: Lens, Spectacle, Non-Custom (Prescription)
Regulation: 21 CFR 886.5844
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: 56
Ingested recalls: 4

Clearances, product code HQG

By decision year

56 clearances under product code HQG with a decision year between 1976 and 1994, 1986 the highest year at 9.

Show the numbers

510(k) clearances under FDA product code HQG by decision year
Year	Clearances
1976	1
1977	4
1978	2
1979	4
1980	3
1981	3
1982	3
1983	1
1984	6
1985	7
1986	9
1987	4
1988	6
1990	1
1992	1
1994	1

Applicants with the most clearances

Product code HQG

Applicants holding the most 510(k) clearances under product code HQG
Applicant	Clearances
American Optical Corp.	4
Aura Lens Products	2
Barnes-Hind, Inc.	2
Gentex Corporation	2
Seiko Optical Products of America, Inc.	2
Techsight Corp.	2
Ancie Laboratories	1
Asahi Optical Co. C/O Rosati Associates, P.C.	1
Automated Lens System	1
B & M Sporting Goods, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 601 companies shown, in name order