Shaser, Inc. is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shaser, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Shaser Skin Beauty Intense Pulsed Light System Family for Acne, Shaser Skin Beauty SkinREJUV Intense, Pulsed Light System Family, SHASER SKIN BEAUTY INTENSE PULSED LIGHT SYSTEM FAMILY
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