Niic U.S.A., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Niic U.S.A., Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Niic U.S.A., Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Redwood City, US.
Historical record: 16 cleared submissions from 1988 to 1990.
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 - Niic U.S.A., Inc.
16 devices
Cleared
Oct 02, 1990
MODEL IS102S ND:YAG SURGICAL LASER SYSTEM
General & Plastic Surgery
145d
Cleared
Aug 14, 1990
MODELS IR103,IR107,IR104,IR205 (ADD'L APPLICATION)
General & Plastic Surgery
153d
Cleared
Jun 29, 1990
NIIC MODEL 15 CARBON-DIOXIDE SURGICAL LASER SYSTEM
General & Plastic Surgery
57d
Cleared
Jun 05, 1990
EXPANDED MARKETING OF MODELS IR104 & IR205 LASERS
General & Plastic Surgery
83d
Cleared
May 24, 1990
NIIC MODEL: DX901 ASPIRATION SYSTEM
Chemistry
128d
Cleared
Jan 23, 1990
NIIC LASER SYSTEM
General & Plastic Surgery
49d
Cleared
Dec 13, 1989
MODEL: IR205 ARTICULATED SURGICAL LASER
General & Plastic Surgery
89d
Cleared
Nov 16, 1989
MODEL NUMBER: IR204 CO2 SURGICAL LASER SYSTEM
General & Plastic Surgery
224d
Cleared
Nov 16, 1989
MODEL IR107 50-WATT CARBON-DIOXIDE SURGICAL LASER
General & Plastic Surgery
87d
Cleared
Nov 16, 1989
MODEL IR103 SURGICAL LASER SYSTEM
General & Plastic Surgery
87d
Cleared
Aug 24, 1989
CO2 SURGICAL LASER SYSTEM
General & Plastic Surgery
77d
Cleared
Nov 02, 1988
CO2 SURGICAL LASER SYSTEM MODEL #IR105
General & Plastic Surgery
111d