Directed Energy, Inc. - FDA 510(k) Cleared Devices
39
Total
38
Cleared
0
Denied
Directed Energy, Inc. has 38 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 38 cleared submissions from 1984 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Directed Energy, Inc. Filter by specialty or product code using the sidebar.
39 devices
Cleared
Mar 21, 1991
SURGICAL CARBON DIOXIDE LASER SYST MODEL 20-CH
General & Plastic Surgery
141d
Cleared
Jun 18, 1990
MODEL 20-CH W/ AR-10A/U OPTICAL ATTACHMENT
General & Plastic Surgery
362d
Cleared
Nov 15, 1988
CARBON DIOXIDE LASER SYSTEM MODEL 20-CX W/ATTACH.
General & Plastic Surgery
75d
Cleared
Sep 09, 1988
MODEL AU-1 ACCESSORY UNIT
General & Plastic Surgery
58d
Cleared
Mar 04, 1988
MODEL 20C W/AN AR-10A/U & RL-20A/U FOR ARTHROSCOP.
General & Plastic Surgery
44d
Cleared
Feb 17, 1988
ORTHO. GAS INSUFFLATOR MODEL IN-2 FOR ARTHRO. SURG
Orthopedic
182d
Cleared
Feb 02, 1988
MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.0 OB/GYN
Obstetrics & Gynecology
341d
Cleared
Feb 02, 1988
MODEL 20-C, RL-20A/U, OB-10A/U
Obstetrics & Gynecology
210d
Cleared
Sep 28, 1987
MODEL 20-C W/AR-10A/U ATTACH. FOR ARTHRO. SURGERY
General & Plastic Surgery
83d
Cleared
Sep 24, 1987
MODEL 20-B W/OB-10A/U ATTACH. FOR EAR, NOSE/THROAT
Ear, Nose, Throat
79d
Cleared
Jun 12, 1987
MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH
Ear, Nose, Throat
106d
Cleared
May 26, 1987
MODEL 20-C W/SA-20A/U OPTICAL ATTACHMENT/SURG USE
General & Plastic Surgery
89d
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