Mnlase, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mnlase, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Mnlase, Inc. has 22 FDA 510(k) cleared general & plastic surgery devices. Based in Minneapolis, US.
Historical record: 22 cleared submissions from 1992 to 1994.
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 - Mnlase, Inc.
22 devices
Cleared
Nov 09, 1994
MODEL 230-SAS LASER DELIVERY PROBE
General & Plastic Surgery
50d
Cleared
Nov 03, 1994
CURVED ENDOPHOTOCOAGULATOR LASER PROBE
General & Plastic Surgery
55d
Cleared
Nov 03, 1994
STRAIGHT ENDOPHOTOCOAGULATOR LASER PROBE
General & Plastic Surgery
55d
Cleared
Nov 03, 1994
MODEL 210-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 210-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 220-SC CURVED ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 220-SS LASER DELIVERY PROBE
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 230-SAC LASER DELIVERY PROBE
General & Plastic Surgery
44d
Cleared
Nov 01, 1994
LASER DELIVERY PROBE
General & Plastic Surgery
60d
Cleared
Nov 01, 1994
CURVD ENDOPHOTOCOGULATOR LASER PROBE
General & Plastic Surgery
53d
Cleared
Nov 01, 1994
MODEL 110-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
42d
Cleared
Nov 01, 1994
MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
42d