510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MVNClass II

Lens, Contact, (Disposable)

21 CFR 886.5925 / Ophthalmic
FDA source (opens on fda.gov)

MVN is the FDA product code for Lens, Contact, (Disposable), a class II device type, regulated under 21 CFR 886.5925. As of , FDA records hold 26 510(k) clearances under this code, the most recent dated , and 16 recalls.

Classification record

Product code
MVN
Device name
Lens, Contact, (Disposable)
Regulation
21 CFR 886.5925
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
26
Ingested recalls
17

Clearances, product code MVN

By decision year
26 clearances under product code MVN with a decision year between 1999 and 2026, 2001 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code MVN by decision year
YearClearances
19993
20014
20021
20031
20053
20064
20071
20082
20111
20131
20152
20202
20261

Applicants with the most clearances

Product code MVN
Applicants holding the most 510(k) clearances under product code MVN
ApplicantClearances
Alcon Laboratories8
Bausch & Lomb Incorporated4
CooperVision, Inc.2
Innova Vision Inc.2
Sauflon Pharmaceuticals, Ltd.2
Yung Sheng Optical Co., Ltd.2
Ciba Vision Johns Creek Mfg.1
Ciba-Geigy Corp.1
Clearlab SG Pte, Ltd.1
Hoya Lamphun Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 91 companies shown, in name order