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

Stimulator, Salivary System

21 CFR 872.5560 / Dental
FDA source (opens on fda.gov)

LTF is the FDA product code for Stimulator, Salivary System, a class II device type, regulated under 21 CFR 872.5560. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 35 recalls.

Classification record

Product code
LTF
Device name
Stimulator, Salivary System
Regulation
21 CFR 872.5560
Device class
Class II
Review panel
Dental
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
35

Clearances, product code LTF

By decision year
2 clearances under product code LTF with a decision year between 2017 and 2018, 2017 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LTF by decision year
YearClearances
20171
20181

Applicants with the most clearances

Product code LTF
Applicants holding the most 510(k) clearances under product code LTF
ApplicantClearances
Saliwell Ltd.2

Companies listing this code with FDA

Companies whose registered establishments list this code