Silver Bay, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Silver Bay, LLC - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Silver Bay, LLC has 5 FDA 510(k) cleared medical devices. Based in Laguna Niguel, US.
Historical record: 5 cleared submissions from 2007 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Silver Bay, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Silver Bay, LLC
5 devices
Cleared
Aug 14, 2012
C100 WRINKLE REDUCTION DEVICE
General & Plastic Surgery
363d
Cleared
Jan 18, 2012
QUASAR CALYPSO
General & Plastic Surgery
257d
Cleared
Sep 17, 2010
BABY QUASAR
General & Plastic Surgery
487d
Cleared
Aug 27, 2010
QUASAR BLUE LIGHT THERAPY SYSTEM
General & Plastic Surgery
247d
Cleared
Oct 15, 2007
QUASAR BLUE LIGHT THERAPY SYSTEM
General & Plastic Surgery
17d