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

Button, Nasal Septal

Unknown
FDA source (opens on fda.gov)

LFB is the FDA product code for Button, Nasal Septal. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
LFB
Device name
Button, Nasal Septal
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
12
Ingested recalls
2

Clearances, product code LFB

By decision year
12 clearances under product code LFB with a decision year between 1978 and 2013, 1987 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LFB by decision year
YearClearances
19781
19821
19851
19861
19872
19901
19921
19971
19981
20011
20131

Applicants with the most clearances

Product code LFB
Applicants holding the most 510(k) clearances under product code LFB
ApplicantClearances
Abco Dealers, Inc.1
Boston Medical Products, Inc.1
Cox-Uphuff Intl.1
Freudenberg Medical, LLC1
Hood Laboratories1
Invotec International, Inc.1
Micromedics, Inc.1
Microtek Medical LLC1
Omega Silicone, Inc.1
Santa Barbara Medco, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code