FRAXEL RE:STORE LASER SYSTEM SYS-SR1500-US

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-09-25 for FRAXEL RE:STORE LASER SYSTEM SYS-SR1500-US manufactured by Solta Medical.

MAUDE Entry Details

Report Number3011423170-2019-00096
MDR Report Key9117681
Report SourceHEALTH PROFESSIONAL
Date Received2019-09-25
Date of Report2019-08-28
Date of Event2019-08-26
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2019-08-28
Date Added to Maude2019-09-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTES PROUD
Manufacturer Street1400 GOODMAN STREET NORTH
Manufacturer CityROCHESTER NY 14609
Manufacturer CountryUS
Manufacturer Postal14609
Manufacturer Phone5853388549
Manufacturer G1SOLTA MEDICAL
Manufacturer Street11720 N CREEK PARKWAY N STE 100
Manufacturer CityBOTHELL WA 98011
Manufacturer CountryUS
Manufacturer Postal Code98011
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameFRAXEL RE:STORE LASER SYSTEM
Generic NamePOWERED LASER SURGICAL INSTRUMENT WITH MICROBEAM
Product CodeONG
Date Received2019-09-25
Model NumberSYS-SR1500-US
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Sequence No1
Device Event Key0
ManufacturerSOLTA MEDICAL
Manufacturer Address11720 N CREEK PARKWAY N STE 10 BOTHELL WA 98011 US 98011

Device Sequence Number: 101

Product Code---
Date Received2019-09-25
Device Sequence No101
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-25

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