Niic U.S.A., Inc.
Niic U.S.A., Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1990.
Top product codes for Niic U.S.A., Inc.
Recent clearances by Niic U.S.A., Inc.
- K902133 — MODEL IS102S ND:YAG SURGICAL LASER SYSTEM
- K901205 — MODELS IR103,IR107,IR104,IR205 (ADD'L APPLICATION)
- K902063 — NIIC MODEL 15 CARBON-DIOXIDE SURGICAL LASER SYSTEM
- K901204 — EXPANDED MARKETING OF MODELS IR104 & IR205 LASERS
- K900185 — NIIC MODEL: DX901 ASPIRATION SYSTEM
- K896988 — NIIC LASER SYSTEM
- K895581 — MODEL: IR205 ARTICULATED SURGICAL LASER
- K892359 — MODEL NUMBER: IR204 CO2 SURGICAL LASER SYSTEM
- K895239 — MODEL IR107 50-WATT CARBON-DIOXIDE SURGICAL LASER
- K895247 — MODEL IR103 SURGICAL LASER SYSTEM
- K894074 — CO2 SURGICAL LASER SYSTEM
- K882951 — CO2 SURGICAL LASER SYSTEM MODEL #IR105
- K882952 — CO2 SURGICAL LASER SYSTEM MODEL #IR106
- K880816 — MODEL 130YZ CO2-YAG SURGICAL LASER SYSTEM
- K880814 — DX101 ULTRASONIC SURGICAL SYSTEM
- K880815 — DX101-T ULTRASONIC SURGICAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.