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

Lenses, Soft Contact, Extended Wear

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

LPM is the FDA product code for Lenses, Soft Contact, Extended Wear, a class III device type, regulated under 21 CFR 886.5925. As of , FDA records hold no 510(k) clearances under this code and 26 recalls.

Classification record

Product code
LPM
Device name
Lenses, Soft Contact, Extended Wear
Regulation
21 CFR 886.5925
Device class
Class III
Review panel
Ophthalmic
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
26

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 43 companies shown, in name order