510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
LYXUnclassified

Media, Corneal Storage

Unknown
FDA source (opens on fda.gov)

LYX is the FDA product code for Media, Corneal Storage. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LYX
Device name
Media, Corneal Storage
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
21
Ingested recalls
0

Clearances, product code LYX

By decision year
21 clearances under product code LYX with a decision year between 1982 and 2025, 1987 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LYX by decision year
YearClearances
19821
19852
19861
19873
19881
19901
19923
19961
20031
20072
20151
20161
20211
20221
20251

Applicants with the most clearances

Product code LYX
Applicants holding the most 510(k) clearances under product code LYX
ApplicantClearances
Al.chi.mi.a. SRL4
Bioclinical Laboratory Services, Inc.3
Chiron Intraoptics3
Northern Scientific, Inc.2
3M Company1
Aurolab1
Bausch + Lomb, Incorporated1
Chen Ophthalmic Laboratories1
Chiron Ophthalmics1
Cilco, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code