Morcher G M B H

FDA Filings

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

FDA Registration(s)
Registration Number9617458
FEI Number1000447964
NameMichael van de Woude
Owner & OperatorMORCHER GMBH
Contact AddressKAPUZINERWEG 12 --
STUTTGART, WURTTEMBERG-BADEN DE-NOTA 70374 DE
Official Correspondent
  • Eric Morcher
  • 49-711-9532040-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2500 Bee Cave Road, Bldg 1, Ste 300
Austin, TX 78746 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Morcher GmbH
 EYEJET® CTR Type 20C Right 2023-09-22
MORCHER GMBH
 FortiEYE CAPSULAR TENSION RINGS, TYPES 14, 14A AND 14C2017-01-26
MORCHER GMBH
 EYEJET INJECTOR2013-05-23
Michael van de Woude [MORCHER GMBH]
Capsular Tension Rings2009-07-14
MORCHER GMBH
 MORCHER CAPSULAR TENSION RINGS2009-05-22
Michael van de Woude [MORCHER GMBH]
Ring Caliper2006-03-06
MORCHER GMBH
 CIONNI CAPSULAR TENSION RINGS2005-10-14
Michael van de Woude [MORCHER GMBH]
ASTI DISC2004-11-01
MORCHER GMBH
 ALCON REFORM CAPSULAR TENSION RING2004-03-15
MORCHER GMBH
 MORCHER CAPSULAR TENSION RING, TYPES 14, 14A AND 14C2003-10-23

Related Finance Registrations
NCAGE CodeCL969MORCHER GMBH
CAGE CodeCL969MORCHER GMBH
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