Shaser, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shaser, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Shaser, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Melrose, US.
Historical record: 10 cleared submissions from 2011 to 2015.
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 - Shaser, Inc.
10 devices
Cleared
May 27, 2015
Shaser Skin Beauty Intense Pulsed Light System Family for Acne
General & Plastic Surgery
111d
Cleared
Feb 13, 2015
Shaser Skin Beauty SkinREJUV Intense, Pulsed Light System Family
General & Plastic Surgery
128d
Cleared
Jul 22, 2014
SHASER SKIN BEAUTY INTENSE PULSED LIGHT SYSTEM FAMILY
General & Plastic Surgery
39d
Cleared
May 16, 2014
LUMENA FH HAIR REMOVAL SYSTEM
General & Plastic Surgery
65d
Cleared
Feb 12, 2014
SHASER V-MINI 2 HAIR REMOVAL SYSTEM
General & Plastic Surgery
118d
Cleared
Nov 26, 2013
SHASER V-MINI RX
General & Plastic Surgery
134d
Cleared
Sep 30, 2013
SHASER HRS2 RX HAIR REMOVAL SYSTEM
General & Plastic Surgery
70d
Cleared
Jun 13, 2013
SHASER V-MINI HAIR REMOVAL SYSTEM
General & Plastic Surgery
161d
Cleared
May 25, 2012
SHASER HRS2 HAIR REMOVAL SYSTEM
General & Plastic Surgery
135d
Cleared
May 18, 2011
SHASER IPL HAIR REMOVAL SYSTEM
General & Plastic Surgery
166d