Wavelight G M B H Pressath

FDA Filings

This page includes the latest FDA filings for Wavelight G M B H Pressath. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3003288808
FEI Number3003288808
NameWAVELIGHT GmbH (Pressath)
Owner & OperatorWAVELIGHT GmbH
Contact AddressAM WOLFSMANTEL 5 --
ERLANGEN DE-NOTA 91058 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressDOELLNITZ 5
PRESSATH Bayern, 92690 DE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WaveLight FS200 Patient Interface 15152019-05-02
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WaveLight FS200 Patient Interface 15152019-05-02
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
Wavelight FS2002016-11-10
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WAVELIGHT FS2002010-11-02
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WAVELIGHT FS2002010-11-02
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
Lifting Table Diagnostic2008-10-24
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
Lifting Table Diagnostic System2008-10-24
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WAVELIGHT EX5002007-12-19
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
ALLEGRETTO WAVE Eye-Q2007-12-19
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
WAVELIGHT EX5002007-10-24
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
ALLEGRETTO WAVE Eye-Q2007-10-24
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
Wavelight Analyzer II2006-06-28
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
ALLEGRO ANALYZER2006-06-28
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
ALLEGRO TOPOLYZER2006-06-28
WAVELIGHT GmbH (Pressath) [WAVELIGHT GmbH]
ALLEGRO TOPOLYZER VARIO2006-06-28

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