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

Locator, Root Apex

Unknown
FDA source (opens on fda.gov)

LQY is the FDA product code for Locator, Root Apex. As of , FDA records hold 46 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LQY
Device name
Locator, Root Apex
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
46
Ingested recalls
0

Clearances, product code LQY

By decision year
46 clearances under product code LQY with a decision year between 1987 and 2026, 1995 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LQY by decision year
YearClearances
19872
19891
19901
19931
19953
19963
19971
19991
20001
20022
20031
20041
20061
20072
20082
20092
20103
20112
20122
20131
20141
20161
20182
20191
20212
20221
20231
20241
20252
20261

Applicants with the most clearances

Product code LQY
Applicants holding the most 510(k) clearances under product code LQY
ApplicantClearances
Medicnrg, Ltd.5
J. Morita USA, Inc.4
S-Denti Co., Ltd.4
Analytic Technology2
Good Doctors Co., Ltd.2
Parkell, Inc.2
Toei Electric Co., Ltd.2
American Medical & Dental Corp.1
Aseptico, Inc.1
Cefla S.C.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 52 companies shown, in name order