Radiancy (Israel) , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radiancy (Israel) , Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Radiancy (Israel) , Ltd. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, US.
Historical record: 11 cleared submissions from 2002 to 2010.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Radiancy (Israel) , Ltd.
11 devices
Cleared
Oct 04, 2010
NO!NO! SKIN
General & Plastic Surgery
35d
Cleared
Dec 03, 2008
NO!NO! SKIN
General & Plastic Surgery
103d
Cleared
Jan 07, 2008
RADIANCY MISTRAL DEVICE
General & Plastic Surgery
140d
Cleared
Mar 22, 2006
RADIANCY CLEARTOUCH LITE ACNE CLEARANCE SYSTEM
General & Plastic Surgery
34d
Cleared
Feb 01, 2006
RADIANCY FACIAL SKINCARE DEVICE
General & Plastic Surgery
99d
Cleared
Jan 26, 2006
RADIANCY SKINSTATION WITH PSORIASIS LIGHT UNIT ASSEMBLY
General & Plastic Surgery
142d
Cleared
Sep 02, 2005
RADIANCY SKINSTATION WITH MODIFIED LIGHT UNIT ADDEMBLY
General & Plastic Surgery
72d
Cleared
Dec 11, 2003
RADIANCY ACNE SYSTEM WITH CLEARTOUCH LIGHT UNIT ASSEMBLY
General & Plastic Surgery
146d
Cleared
Oct 24, 2003
SPR SYSTEM
General & Plastic Surgery
23d
Cleared
Jun 19, 2003
SKINSTATION
General & Plastic Surgery
90d
Cleared
Jun 13, 2002
SPATOUCH PHOTOEPILATION SYSTEM
General & Plastic Surgery
90d