MSSClass I

Folders And Injectors, Intraocular Lens (Iol)

21 CFR 886.4300 / Ophthalmic

MSS is the FDA product code for Folders And Injectors, Intraocular Lens (Iol), a class I device type, regulated under 21 CFR 886.4300. As of 2026-09-10, FDA records hold 63 510(k) clearances under this code, the most recent dated 2026-06-10, and 5 recalls.

Classification record

Product code: MSS
Device name: Folders And Injectors, Intraocular Lens (Iol)
Regulation: 21 CFR 886.4300
Device class: Class I
Review panel: Ophthalmic
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 63
Ingested recalls: 5

Clearances, product code MSS

By decision year

63 clearances under product code MSS with a decision year between 1997 and 2026, 2006 the highest year at 5.

Show the numbers

510(k) clearances under FDA product code MSS by decision year
Year	Clearances
1997	1
1998	1
2000	1
2001	2
2003	2
2004	1
2005	1
2006	5
2007	2
2008	5
2009	5
2010	2
2011	2
2012	2
2013	5
2014	5
2015	3
2016	2
2017	3
2018	1
2019	3
2020	2
2021	1
2023	3
2024	1
2025	1
2026	1

Applicants with the most clearances

Product code MSS

Applicants holding the most 510(k) clearances under product code MSS
Applicant	Clearances
Bausch & Lomb Incorporated	12
Lenstec, Inc.	5
Medicel AG	5
RxSight Inc.	5
Staar Surgical AG	5
AST Products, Inc.	4
Rayner Intraocular Lenses Limited	4
Advanced Medical Optics, Inc.	3
Alcon Laboratories	3
Duckworth & Kent, Ltd.	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 33 companies shown, in name order