Surgilase, Inc. is one of 6965 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgilase, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASE, SURGILASE FIBERLASE CO2 LASER WAVEGUIDE, SURGILASE SL 150 SURGICAL LASER SYSTEM
19
Total
19
Cleared
0
Denied
Surgilase, Inc. has 19 FDA 510(k) cleared general & plastic surgery devices. Based in Providence, US.
Historical record: 19 cleared submissions from 1985 to 1993.
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 - Surgilase, Inc.
19 devices
Cleared
Oct 15, 1993
SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASE
General & Plastic Surgery
149d
Cleared
Apr 15, 1993
SURGILASE FIBERLASE CO2 LASER WAVEGUIDE
General & Plastic Surgery
226d
Cleared
Feb 21, 1991
SURGILASE SL 150 SURGICAL LASER SYSTEM
General & Plastic Surgery
107d
Cleared
Dec 07, 1990
SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEM
General & Plastic Surgery
86d
Cleared
Jun 29, 1990
SURGILASE YAG 100 SURGICAL LASER SYSTEM
General & Plastic Surgery
50d
Cleared
May 01, 1990
SURGILASE YAG 100 IN ORTHOPEDIC SURGERY
General & Plastic Surgery
83d
Cleared
Apr 26, 1990
SURGILASE SL50 SURGICAL LASER SYSTEM
General & Plastic Surgery
43d
Cleared
Apr 26, 1990
SURGILASE CO2 SURGICAL LASER SYSTEMS MODEL SL120
General & Plastic Surgery
43d
Cleared
Nov 14, 1989
SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY
General & Plastic Surgery
119d
Cleared
Aug 07, 1989
SURGILASE 25, 40, 45, 55, 60, 80, 100 LASER
General & Plastic Surgery
21d
Cleared
Apr 06, 1989
SURGILASE YAG 100 SURGICAL ND:YAG LASER/GEN SURG
General & Plastic Surgery
22d
Cleared
Jan 24, 1989
SURGILASE YAG 100 SURGIPROBES & SURGISCALPEL
General & Plastic Surgery
118d