Esc Medical Systems , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Esc Medical Systems , Ltd. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Esc Medical Systems , Ltd. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Needham, US.
Historical record: 10 cleared submissions from 1996 to 2000.
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 - Esc Medical Systems , Ltd.
10 devices
Cleared
Feb 24, 2000
ESC INTENSE PULSED LIGHT SYSTEMS: EPILIGHT AND MULTILIGHT
General & Plastic Surgery
90d
Cleared
Jan 27, 2000
EPILIGHT HAIR REMOVAL SYSTEM, PHOTODERM HR SYSTEM
General & Plastic Surgery
232d
Cleared
Feb 04, 1999
DIODE LASER
General & Plastic Surgery
233d
Cleared
May 20, 1998
PHOTODERM HR SYSTEM
General & Plastic Surgery
169d
Cleared
Apr 15, 1998
ND: YAG ACCESSORY FOR PHOTODERM SYSTEM
General & Plastic Surgery
63d
Cleared
Oct 28, 1997
DERMA K LASER SYSTEM
General & Plastic Surgery
85d
Cleared
Oct 24, 1997
DERMASCAN SURGICAL LASER SCANNER
General & Plastic Surgery
144d
Cleared
Jul 07, 1997
EPILIGHT HAIR REMOVAL SYSTEM
General & Plastic Surgery
322d
Cleared
Apr 11, 1997
DERMA 20 LASER SYSTEM
General & Plastic Surgery
169d
Cleared
Sep 11, 1996
PHOTODERM PL.
General & Plastic Surgery
198d