ClearanceBrief
Company ยท TW

Lightmed Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2019. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
HQFLaser, Ophthalmic11
IYOSystem, Imaging, Pulsed Echo, Ultrasonic2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 1, 2019K183173LIGHTMED Ultrasound System
Lightmed USA, Inc.
IYO
Apr 13, 2018K170761LIGHTSonic BUBM
Lightmed USA, Inc.
IYO
Jun 15, 2016K152688LightLas Multi-Wavelength Medical Laser System
Lightmed Corporation, TW
HQF
Feb 27, 2015K142172LIGHTMED TRUSCAN 577
Lightmed Corp., TW
HQF
Sep 26, 2013K124043LIGHTLAS FAMILY OF MULTI-WAVELENGTH MEDICAL LASER SYSTEM
Lightmed Corp., TW
HQF
Nov 3, 2011K103547LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM
Lightmed Corp., TW
HQF
Sep 28, 2009K091981LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER
Lightmed Corp., TW
HQF
Sep 18, 2009K091534LIGHTLAS MODEL 532
Lightmed Corp., TW
HQF
Aug 13, 2009K090774LIGHTLAS SELECTOR
Lightmed Corp., TW
HQF
Sep 20, 2007K063297LIGHTLAS 561 OPTHALMIC PHOTOCOAGULATOR
Lightmed Corp.
HQF
Aug 8, 2002K021538LIGHTLAS 810 INFRARED LASER PHOTOCOAGULATOR
Lightmed Corp., TW
HQF
Aug 22, 2001K010372LIGHTLAS 532 PHOTOCOAGULATOR
Lightmed Corp., TW
HQF

Latest recalls

DateFirm and productCodeLinked 510(k)
Dec 17, 2003LightMed USA Inc
Model LightLas 532 Opthalmic Photocoagulator Laser
Terminated
HQFK010372
K990075
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