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

Implant, Dermal, For Aesthetic Use

Unknown
FDA source (opens on fda.gov)

LMH is the FDA product code for Implant, Dermal, For Aesthetic Use, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 7 recalls.

Classification record

Product code
LMH
Device name
Implant, Dermal, For Aesthetic Use
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
7

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 29 companies shown, in name order