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

Lens, Intraocular, Toric Optics

21 CFR 886.3600 / Ophthalmic
FDA source (opens on fda.gov)

MJP is the FDA product code for Lens, Intraocular, Toric Optics, a class III device type, regulated under 21 CFR 886.3600. As of , FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code
MJP
Device name
Lens, Intraocular, Toric Optics
Regulation
21 CFR 886.3600
Device class
Class III
Review panel
Ophthalmic
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
4

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order