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

Lenses, Soft Contact, Daily Wear

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

LPL is the FDA product code for Lenses, Soft Contact, Daily Wear, a class II device type, regulated under 21 CFR 886.5925. As of , FDA records hold 486 510(k) clearances under this code, the most recent dated , and 70 recalls.

Classification record

Product code
LPL
Device name
Lenses, Soft Contact, Daily Wear
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
487
Ingested recalls
70

Clearances, product code LPL

By decision year
487 clearances under product code LPL with a decision year between 1994 and 2026, 2001 the highest year at 33.
Show the numbers
510(k) clearances under FDA product code LPL by decision year
YearClearances
199417
199516
199625
199726
199821
199932
200024
200133
200217
200317
200413
200514
20065
20073
200810
20096
20109
201112
201212
201317
201415
201512
201621
20179
201821
201911
202010
20218
20229
202310
202412
202512
20268

Applicants with the most clearances

Product code LPL
Applicants holding the most 510(k) clearances under product code LPL
ApplicantClearances
CooperVision, Inc.37
Alcon Laboratories36
Bausch & Lomb Incorporated18
Johnson & Johnson Vision Care, Inc.16
Pegavision Corporation14
Unilens Corp., USA14
St. Shine Optical Co., Ltd.11
Visco Vision Inc.11
Alden Optical Labs., Inc.10
Benz Research and Development LLC10

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 121 companies shown, in name order