Medical Device Manufacturer · US , Milford , MA

Laser Engineering, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1988

Total

Cleared

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.

FDA 510(k) Regulatory Record - Laser Engineering, Inc.

18 devices

1-12 of 18

Cleared Sep 22, 2022

Dual Switch

K211605 · GEX

General & Plastic Surgery · 485d

Cleared Oct 22, 2014

DUAL SWITCH

K141908 · GEX

General & Plastic Surgery · 99d

Cleared May 07, 1993

MICROMANIPULATOR

K924457 · GEX

General & Plastic Surgery · 247d

Cleared Nov 13, 1991

UNIVERSAL COUPLER, LAPAROSCOPIC ACCESSORY

K912247 · GCJ

General & Plastic Surgery · 176d

Cleared Sep 23, 1991

BIPURE 1000

K912347 · FYD

General Hospital · 118d

Cleared Aug 16, 1991

02-10,001

K910062 · GEX

General & Plastic Surgery · 219d

Cleared Jun 07, 1991

COMPULSE CO2 SURGICAL LASER SYS.

K911852 · GEX

General & Plastic Surgery · 42d

Cleared Apr 22, 1991

MD CO2 SURGICAL LASER SYSTEM/GEN. SURGERY AND ORTH

K905676 · GEX

General & Plastic Surgery · 125d

Cleared Aug 05, 1988

GL-35 COLPOSCOPIC LASER SYSTEM

K875314 · HHR

Obstetrics & Gynecology · 220d

Cleared Jun 03, 1988

MODEL MD-25 CO2 LASER FOR DERMA./PLASTIC SURGERY

K881580 · GEX

General & Plastic Surgery · 53d

Cleared Jun 03, 1988

MODEL MD-45 CO2 LASER FOR OB-GYN & UROLOGICAL USE

K881581 · GEX

General & Plastic Surgery · 53d

Cleared Jun 03, 1988

MODEL MD-45 CO2 LASER FOR DERMATOLOGY/PODIATRY USE

K881582 · GEX

General & Plastic Surgery · 53d

Laser Engineering, Inc. - FDA 510(k) Cleared Devices

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