HPQClass II

Headlamp, Operating, Ac-Powered

21 CFR 886.4335 / Ophthalmic

HPQ is the FDA product code for Headlamp, Operating, Ac-Powered, a class II device type, regulated under 21 CFR 886.4335. As of 2026-09-10, FDA records hold 5 510(k) clearances under this code, the most recent dated 1995-07-14, and no recalls.

Classification record

Product code: HPQ
Device name: Headlamp, Operating, Ac-Powered
Regulation: 21 CFR 886.4335
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: 5
Ingested recalls: 0

Clearances, product code HPQ

By decision year

5 clearances under product code HPQ with a decision year between 1982 and 1995, 1986 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code HPQ by decision year
Year	Clearances
1982	1
1986	2
1995	2

Applicants with the most clearances

Product code HPQ

Applicants holding the most 510(k) clearances under product code HPQ
Applicant	Clearances
Keeler Instruments, Inc.	2
Kelleher Corp.	1
Neitz Instruments Company, Ltd.	1
Welch Allyn Inc	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code HPQ

Recent recalls

Product code HPQ

FDA records show no recalls under product code HPQ.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)