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

Saliva, Artificial

Unknown
FDA source (opens on fda.gov)

LFD is the FDA product code for Saliva, Artificial. As of , FDA records hold 50 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
LFD
Device name
Saliva, Artificial
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
50
Ingested recalls
6

Clearances, product code LFD

By decision year
50 clearances under product code LFD with a decision year between 1981 and 2026, 2015 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code LFD by decision year
YearClearances
19811
19821
19841
19851
19881
19991
20011
20032
20041
20051
20062
20072
20093
20101
20113
20122
20132
20155
20173
20185
20193
20201
20212
20231
20242
20251
20261

Applicants with the most clearances

Product code LFD
Applicants holding the most 510(k) clearances under product code LFD
ApplicantClearances
Glaxosmithkline Consumer Healthcare (Gskch)3
Kingswood Laboratories, Inc.3
Laclede, Inc.3
Procter & Gamble Co.3
Elevate Oral Care, LLC2
Eusa Pharma (Uk) Limited2
Inpharma A.S.2
Bartor Pharmacal Co., Inc.1
Bio Cosmetics S.L.1
Bio-X Healthcare S.A.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 39 companies shown, in name order