DeviceClearance

Product code MMX— Cardiovascular

LimFlow V-Ceiver

Classification name
Device, Percutaneous Retrieval
Device class
Class 2
Regulation
21 CFR 870.5150
Advisory panel
Cardiovascular
Total cleared
32
First cleared
Most recent

Market context for product code MMX

FDA has cleared 32 devices under product code MMX between 2002 and 2025, filed by 19 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code MMX

Adverse events under product code MMX

product code MMX
Death
3
Total
3

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code MMX

Data sourced from openFDA. This site is unofficial and independent of the FDA.