Coherent Medical Group is one of 13679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coherent Medical Group - FDA 510(k) Cleared Devices
Recent clearances: COHERENT ULTRAPULSE CO2 SURGICAL LASERS, COHERENT VERSAPULSE AESTHETIC SURGICAL LASERS, COHERENT VERSAPULSE 2.1 HOLMIUM SURGICAL LASERS
27
Total
24
Cleared
0
Denied
Coherent Medical Group has 24 FDA 510(k) cleared general & plastic surgery devices. Based in Palo Alto, US.
Historical record: 24 cleared submissions from 1985 to 1997.
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.
510(k) submissions have been managed by Boston Scientific as regulatory consultant.
FDA 510(k) Regulatory Record - Coherent Medical Group
27 devices
Cleared
Jan 22, 1997
COHERENT ULTRAPULSE CO2 SURGICAL LASERS
General & Plastic Surgery
149d
Cleared
Apr 01, 1996
COHERENT VERSAPULSE AESTHETIC SURGICAL LASERS
General & Plastic Surgery
90d
Cleared
May 02, 1994
COHERENT VERSAPULSE 2.1 HOLMIUM SURGICAL LASERS
General & Plastic Surgery
318d
Cleared
Sep 29, 1993
COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERS
General & Plastic Surgery
436d
Cleared
Sep 22, 1993
NOVUS MULTIWAVELENGTH
General & Plastic Surgery
121d
Cleared
Jul 28, 1993
ACCULITE(TM) OTOPROBE
General & Plastic Surgery
153d
Cleared
Jul 21, 1992
COHERENT VERSAPULSE(TM) 2.1XE/2.1L HOLMI SURG LASE
General & Plastic Surgery
309d
Cleared
May 06, 1992
VERSAPULSE(TM) TWOPOINTONE/XE HOLMIUM SURG LASERS
General & Plastic Surgery
181d
Cleared
Oct 08, 1991
COHERENT NOVUS 3000 ARGON PHOTOCOAGULATOR
General & Plastic Surgery
85d
Cleared
Sep 25, 1991
COHERENT HOLMIUM:YAG SURGICAL LASER
General & Plastic Surgery
264d
Cleared
Aug 13, 1991
ULTRAPULSE(TM) CARBON DIOXIDE SURGICAL LASER
General & Plastic Surgery
98d
Cleared
Jun 15, 1989
COHERENT MARIE ARGON PHOTOCOAGULATOR
Ophthalmic
28d