HPFClass I

Aid, Vision, Electronic, Ac-Powered

21 CFR 886.5900 / Ophthalmic

HPF is the FDA product code for Aid, Vision, Electronic, Ac-Powered, a class I device type, regulated under 21 CFR 886.5900. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1986-10-31, and no recalls.

Classification record

Product code: HPF
Device name: Aid, Vision, Electronic, Ac-Powered
Regulation: 21 CFR 886.5900
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: 1
Ingested recalls: 0

Clearances, product code HPF

By decision year

1 clearance under product code HPF with a decision year between 1986 and 1986, 1986 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code HPF by decision year
Year	Clearances
1986	1

Applicants with the most clearances

Product code HPF

Applicants holding the most 510(k) clearances under product code HPF
Applicant	Clearances
Sensory Aids Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code HPF

K863993Class IVts Reporter or Vts LinkSensory Aids Corp. / cleared 1986-10-31

Recent recalls

Product code HPF

FDA records show no recalls under product code HPF.

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)