NAAClass III

Lens, Intraocular, Accommodative

21 CFR 886.3600 / Ophthalmic

NAA is the FDA product code for Lens, Intraocular, Accommodative, a class III device type, regulated under 21 CFR 886.3600. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: NAA
Device name: Lens, Intraocular, Accommodative
Regulation: 21 CFR 886.3600
Device class: Class III
Review panel: Ophthalmic
Submission type: PMA
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code NAA

FDA records hold no clearances under product code NAA.

Recent recalls

Product code NAA

Z-0445-2012Bausch + Lomb voluntary initiated the recall due to a physician complaint of haze on the Crystalens AO which was visualized using...Bausch and Lomb, Incorporated / initiated 2011-11-14 / 62 units

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)