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

Implant, Intragastric For Morbid Obesity

Unknown
FDA source (opens on fda.gov)

LTI is the FDA product code for Implant, Intragastric For Morbid Obesity, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 26 recalls.

Classification record

Product code
LTI
Device name
Implant, Intragastric For Morbid Obesity
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
26

Companies listing this code with FDA

Companies whose registered establishments list this code