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

Plug, Punctum

Unknown
FDA source (opens on fda.gov)

LZU is the FDA product code for Plug, Punctum. As of , FDA records hold 49 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
LZU
Device name
Plug, Punctum
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
49
Ingested recalls
4

Clearances, product code LZU

By decision year
49 clearances under product code LZU with a decision year between 1989 and 2024, 1995 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code LZU by decision year
YearClearances
19894
19902
19913
19921
19955
19962
19974
19982
19991
20003
20025
20031
20042
20051
20062
20091
20143
20151
20161
20171
20191
20222
20241

Applicants with the most clearances

Product code LZU
Applicants holding the most 510(k) clearances under product code LZU
ApplicantClearances
Lacrimedics, Inc.10
Oasis Medical, Inc.6
Grace Medical, Inc.5
Fci Ophthalmics, Inc.3
G.W.B. Intl., Ltd.3
Odyssey Medical, Inc.3
Advanced Vision Science, Inc.2
Visitec Co.2
Alcon, Inc.1
Alphamed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 26 companies shown, in name order