Inovel, LLC is one of 16442 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inovel, LLC - FDA 510(k) Cleared Devices
Recent clearances: INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS, MODELS MFRN95-S, MFRN95-XS, MFRN95-ML, MFRN95-A, INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS, INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS & SURGICAL MASKS
5
Total
5
Cleared
0
Denied
Inovel, LLC has 5 FDA 510(k) cleared medical devices. Based in Culver City, US.
Historical record: 5 cleared submissions from 2004 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Inovel, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Entela, Inc..
FDA 510(k) Regulatory Record - Inovel, LLC
5 devices
Cleared
Jan 12, 2007
INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS, MODELS...
General Hospital
24d
Cleared
Oct 24, 2006
INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS
General Hospital
47d
Cleared
Jul 12, 2006
INOVEL HEALTH CARE N95 PARTICULATE RESPIRATORS & SURGICAL MASKS
General Hospital
12d
Cleared
May 19, 2005
INOVEL HEALTH CARE MODEL N95 PARTICULATE RESPIRATORS AND SURGICAL MASKS
General Hospital
10d
Cleared
Sep 30, 2004
INOVEL HEALTH CARE N95 PARTICULATE RESPIRATOR AND SURGICAL MASK, MODELS...
General Hospital
38d