Laser Engineering, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Laser Engineering, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Milford, US.
Last cleared in 2022. Active since 1988.
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.
18 devices
Cleared
Sep 22, 2022
Dual Switch
General & Plastic Surgery
485d
Cleared
Oct 22, 2014
DUAL SWITCH
General & Plastic Surgery
99d
Cleared
May 07, 1993
MICROMANIPULATOR
General & Plastic Surgery
247d
Cleared
Nov 13, 1991
UNIVERSAL COUPLER, LAPAROSCOPIC ACCESSORY
General & Plastic Surgery
176d
Cleared
Sep 23, 1991
BIPURE 1000
General Hospital
118d
Cleared
Aug 16, 1991
02-10,001
General & Plastic Surgery
219d
Cleared
Jun 07, 1991
COMPULSE CO2 SURGICAL LASER SYS.
General & Plastic Surgery
42d
Cleared
Apr 22, 1991
MD CO2 SURGICAL LASER SYSTEM/GEN. SURGERY AND ORTH
General & Plastic Surgery
125d
Cleared
Aug 05, 1988
GL-35 COLPOSCOPIC LASER SYSTEM
Obstetrics & Gynecology
220d
Cleared
Jun 03, 1988
MODEL MD-25 CO2 LASER FOR DERMA./PLASTIC SURGERY
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-45 CO2 LASER FOR OB-GYN & UROLOGICAL USE
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-45 CO2 LASER FOR DERMATOLOGY/PODIATRY USE
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-25 CO2 LASER FOR EAR, NOSE & THROAT
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-45 CO2 LASER FOR NEUROSURGERY USE
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-25 CO2 LASER FOR NEUROSURGERY USE
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-45 CO2 LASER FOR ENT APPLICATIONS
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-25 CO2 LASER FOR PODIATRY APPLICATIONS
General & Plastic Surgery
53d
Cleared
Jun 03, 1988
MODEL MD-25 LASER FOR SURGICAL USE
General & Plastic Surgery
53d