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Data / Medical devices / Germany / Morcher GMBH

Morcher GMBH: FDA-registered device maker in STUTTGART Baden-Wurttemberg, Germany, 1 PMA approval

Morcher GMBH is registered with the FDA (registration 9617458) in STUTTGART Baden-Wurttemberg, Germany. It lists 3 device types. The FDA files 1 PMA approval under its listings, the newest dated October 23, 2003. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9617458
FEI number
1000447964
Address
Kapuzinerweg 12, STUTTGART Baden-Wurttemberg, Germany, D-70374
Owner or operator
MORCHER GMBH (9035333)
Roles
Manufacturer
First device listed
January 21, 2000
Registered through
2026
Brand names listed
Capsular Tension Rings, Ring Caliper

Devices it lists

DeviceProduct codeClassRoleSource
Clip, Iris RetractorHOC1Manufactureraccessdata.fda.gov
Ring, EndocapsularMRJ3Manufactureraccessdata.fda.gov
Ring, Ophthalmic (Flieringa)HNH1Manufactureraccessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
October 23, 2003P010059MORCHER CAPSULAR TENSION RING, TYPES 14, 14A AND 14CMRJ10November 4, 2024accessdata.fda.gov

Compare with other makers

Updated November 4, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.