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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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238 records meeting your search criteria returned- Product Code: LZS Product Problem: Device Displays Incorrect Message Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 05/06/2021
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 09/30/2020
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 08/06/2020
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 07/16/2020
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 12/17/2019
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 11/08/2019
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 11/04/2019
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 10/28/2019
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 10/24/2019
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 10/16/2019
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