HJJClass I

Lens, Fresnel, Flexible, Diagnostic

21 CFR 886.1390 / Ophthalmic

HJJ is the FDA product code for Lens, Fresnel, Flexible, Diagnostic, a class I device type, regulated under 21 CFR 886.1390. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: HJJ
Device name: Lens, Fresnel, Flexible, Diagnostic
Regulation: 21 CFR 886.1390
Device class: Class I
Review panel: Ophthalmic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code HJJ

FDA records hold no clearances under product code HJJ.

Recent recalls

Product code HJJ

FDA records show no recalls under product code HJJ.

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)