FDA.reportPublic FDA data

SIE AG, Surgical Instrument Engineering

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30111977453011197725SIE AG, Surgical Instrument Engineering1N2020-04-25Erlenstrasse 31 Bruegg Bern CH CH-2555

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
07640167750023FEMTO LDV - Z68667084490usa@ziemergroup.com
07640167750030FEMTO LDV - Z48667084490usa@ziemergroup.com
07640167750047FEMTO LDV - Z28667084490usa@ziemergroup.com
07640167750573FEMTO - Z8 NEO8667084490usa@ziemergroup.com
07640167751334Procedure Pack Z8 - Procedure Pack for Cataract Surgery SLIM8667084490usa@ziemergroup.com
07640167751341Procedure Pack Z8 - Procedure Pack Corneal Surgery 8.5 SLIM8667084490usa@ziemergroup.com
07640167751358Procedure Pack Z8 - Procedure Pack Corneal Surgery 9.0 SLIM8667084490usa@ziemergroup.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1739271438327686K150323FEMTO LDV Z8 Surgical LaserOOE2015-10-23
1739272064272211K112154FEMTO LDVHQF2012-03-16
1739271740501603K053511DA VINCI FEMTOSECOND SURGICAL LASERGEX2006-03-10
1739271863982926

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OOE12015-10-23
HQF12012-03-16
GEX12006-03-10

PMN#

GUDID#

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