Laser Engineering, Inc.
Laser Engineering, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2022.
Top product codes for Laser Engineering, Inc.
Recent clearances by Laser Engineering, Inc.
- K211605 — Dual Switch
- K141908 — DUAL SWITCH
- K924457 — MICROMANIPULATOR
- K912247 — UNIVERSAL COUPLER, LAPAROSCOPIC ACCESSORY
- K912347 — BIPURE 1000
- K910062 — 02-10,001
- K911852 — COMPULSE CO2 SURGICAL LASER SYS.
- K905676 — MD CO2 SURGICAL LASER SYSTEM/GEN. SURGERY AND ORTH
- K875314 — GL-35 COLPOSCOPIC LASER SYSTEM
- K881580 — MODEL MD-25 CO2 LASER FOR DERMA./PLASTIC SURGERY
- K881581 — MODEL MD-45 CO2 LASER FOR OB-GYN & UROLOGICAL USE
- K881582 — MODEL MD-45 CO2 LASER FOR DERMATOLOGY/PODIATRY USE
- K881583 — MODEL MD-25 CO2 LASER FOR EAR, NOSE & THROAT
- K881584 — MODEL MD-45 CO2 LASER FOR NEUROSURGERY USE
- K881585 — MODEL MD-25 CO2 LASER FOR NEUROSURGERY USE
- K881586 — MODEL MD-45 CO2 LASER FOR ENT APPLICATIONS
- K881587 — MODEL MD-25 CO2 LASER FOR PODIATRY APPLICATIONS
- K881588 — MODEL MD-25 LASER FOR SURGICAL USE
Data sourced from openFDA. This site is unofficial and independent of the FDA.