Ventus Medical, Inc.

Ventus Medical, Inc. holds 5 FDA 510(k) medical device clearances, first cleared 2008, most recent 2012.

Top product codes for Ventus Medical, Inc.

Recent clearances by Ventus Medical, Inc.

K120665 — INVENT SNORING DEVICECode LWF·2012-06-12
K102404 — PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50)Code OHP·2010-12-02
K090398 — PROVENT PROFESSIONAL SLEEP APNEA THERAPYCode OHP·2009-04-03
K080983 — PROVENT NASAL CANNULACode MNR·2008-08-07
K071560 — PROVENT NASAL DILATOR, MODEL BR2Code OHP·2008-02-08

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