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Ventus Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K120665INVENT SNORING DEVICEJune 12, 2012
K102404PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PRODecember 2, 2010
K090398PROVENT PROFESSIONAL SLEEP APNEA THERAPYApril 3, 2009
K080983PROVENT NASAL CANNULAAugust 7, 2008
K071560PROVENT NASAL DILATOR, MODEL BR2February 8, 2008