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Data / Medical devices / Germany / Geuder AG

Geuder AG: FDA-registered device maker in HEIDELBERG Baden-Wurttemberg, Germany, 1 510(k) clearance

Geuder AG is registered with the FDA (registration 9616245) in HEIDELBERG Baden-Wurttemberg, Germany. It lists 28 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 4, 2000. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Geuder AG
FDA registration number
9616245
FEI number
3003408840
Address
Hertzstrasse 4, HEIDELBERG Baden-Wurttemberg, Germany, D-69126
Owner or operator
GEUDER AG (9024476)
Roles
Specification developer
First device listed
September 18, 1996
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Caliper, OphthalmicHOE1Specification developeraccessdata.fda.gov
Cannula, OphthalmicHMX1Specification developeraccessdata.fda.gov
Cannula, Trocar, OphthalmicNGY1Specification developeraccessdata.fda.gov
Clamp, Eyelid, OphthalmicHOD1Specification developeraccessdata.fda.gov
Clamp, Muscle, OphthalmicHOB1Specification developeraccessdata.fda.gov
Clip, Iris RetractorHOC1Specification developeraccessdata.fda.gov
Curette, OphthalmicHNZ1Specification developeraccessdata.fda.gov
Depressor, OrbitalHNX1Specification developeraccessdata.fda.gov
Device, Irrigation, Ocular SurgeryKYG1Specification developeraccessdata.fda.gov
Forceps, OphthalmicHNR1Specification developeraccessdata.fda.gov
Hook, OphthalmicHNQ1Specification developeraccessdata.fda.gov
Injector, Capsular Tension RingNCE1Specification developeraccessdata.fda.gov
Knife, OphthalmicHNN1Specification developeraccessdata.fda.gov
Magnet, PermanentHPN1Specification developeraccessdata.fda.gov
Marker, OcularHMR1Specification developeraccessdata.fda.gov
Probe, LachrymalHNL1Specification developeraccessdata.fda.gov
Probe, TrabeculotomyHNK1Specification developeraccessdata.fda.gov
Punch, Corneo-ScleralHNJ1Specification developeraccessdata.fda.gov
Retractor, OphthalmicHNI1Specification developeraccessdata.fda.gov
Ring, Ophthalmic (Flieringa)HNH1Specification developeraccessdata.fda.gov
Ruler, Nearpoint (Punctometer)HLE1Specification developeraccessdata.fda.gov
Scissors, OphthalmicHNF1Specification developeraccessdata.fda.gov
Snare, EnucleatingHNE1Specification developeraccessdata.fda.gov
Spatula, OphthalmicHND1Specification developeraccessdata.fda.gov
Specula, OphthalmicHNC1Specification developeraccessdata.fda.gov
Spoon, OphthalmicHNB1Specification developeraccessdata.fda.gov
Spud, OphthalmicHNA1Specification developeraccessdata.fda.gov
Trephine, Manual, OphthalmicHRH1Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 4, 2000K001125GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RINGNCESubstantially EquivalentGeuder GmbHaccessdata.fda.gov

Compare with other makers

Updated October 4, 2000. 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.