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Data / Medical devices / Germany / Dewimed Medizintechnik GMBH

Dewimed Medizintechnik GMBH: FDA-registered device maker in TUTTLINGEN Baden-Wurttemberg, Germany, 1 510(k) clearance

Dewimed Medizintechnik GMBH is registered with the FDA (registration 3000286616) in TUTTLINGEN Baden-Wurttemberg, Germany. It lists 53 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2006. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3000286616
Address
Unter Hasslen 14, TUTTLINGEN Baden-Wurttemberg, Germany, D-78532
Owner or operator
DEWIMED Medizintechnik GmbH (9030270)
Roles
Manufacturer
First device listed
May 5, 1997
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
ArthroscopeHRX2Manufactureraccessdata.fda.gov
Cannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl AcetalMXY1Manufactureraccessdata.fda.gov
Chisel, Bone, SurgicalEML1Manufactureraccessdata.fda.gov
Chisel, Osteotome, SurgicalEMM1Manufactureraccessdata.fda.gov
Chisel, Surgical, ManualFZO1Manufactureraccessdata.fda.gov
ClampHXD1Manufactureraccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Manufactureraccessdata.fda.gov
Clip, Lens, Trial, OphthalmicHPB1Manufactureraccessdata.fda.gov
Curette, Surgical, DentalEMK1Manufactureraccessdata.fda.gov
Curette, Surgical, General UseFZS1Manufactureraccessdata.fda.gov
Cutter, SurgicalFZT1Manufactureraccessdata.fda.gov
Dissector, Surgical, General & Plastic SurgeryGDI1Manufactureraccessdata.fda.gov
Elevator, Surgical, DentalEMJ1Manufactureraccessdata.fda.gov
Elevator, Surgical, General & Plastic SurgeryGEG1Manufactureraccessdata.fda.gov
File, Bone, SurgicalEMI1Manufactureraccessdata.fda.gov
File, Surgical, General & Plastic SurgeryGEO1Manufactureraccessdata.fda.gov
ForcepsHTD1Manufactureraccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Manufactureraccessdata.fda.gov
Forceps, Rongeur, SurgicalEMH1Manufactureraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Manufactureraccessdata.fda.gov
Gauge, DepthHTJ1Manufactureraccessdata.fda.gov
Hammer, SurgicalFZY1Manufactureraccessdata.fda.gov
Hemostat, SurgicalEMD1Manufactureraccessdata.fda.gov
Hook, Surgical, General & Plastic SurgeryGDG1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Manufactureraccessdata.fda.gov
Instrument, Surgical, Non-PoweredHAO1Manufactureraccessdata.fda.gov
Instruments, Surgical, CardiovascularDWS1Manufactureraccessdata.fda.gov
Knife, SurgicalEMF1Manufactureraccessdata.fda.gov
Lamp, SurgicalFTD2Manufactureraccessdata.fda.gov
Light, Surgical, Ceiling MountedFSY2Manufactureraccessdata.fda.gov
Mallet, Surgical, General & Plastic SurgeryGFJ1Manufactureraccessdata.fda.gov
Marker, OcularHMR1Manufactureraccessdata.fda.gov
Mirror, MouthEAX1Manufactureraccessdata.fda.gov
Needle, Suturing, DisposableGAB1Manufactureraccessdata.fda.gov
Pelvimeter, ExternalHER1Manufactureraccessdata.fda.gov
Pliers, SurgicalHTC1Manufactureraccessdata.fda.gov
Probe, LachrymalHNL1Manufactureraccessdata.fda.gov
Probe, PeriodonticEIX1Manufactureraccessdata.fda.gov
Punch, Biopsy, SurgicalEME1Manufactureraccessdata.fda.gov
Punch, SurgicalLRY1Manufactureraccessdata.fda.gov
RaspHTR1Manufactureraccessdata.fda.gov
Rasp, Surgical, General & Plastic SurgeryGAC1Manufactureraccessdata.fda.gov
Retainer, Screw Expansion, OrthodonticDYJ1Manufactureraccessdata.fda.gov
RetractorGAD1Manufactureraccessdata.fda.gov
Scissors, General, SurgicalLRW1Manufactureraccessdata.fda.gov
Scissors, OphthalmicHNF1Manufactureraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Manufactureraccessdata.fda.gov
Snare, SurgicalGAE1Manufactureraccessdata.fda.gov
Spatula, Surgical, General & Plastic SurgeryGAF1Manufactureraccessdata.fda.gov
Speculum, Vaginal, MetalHDF1Manufactureraccessdata.fda.gov
Tape, Measuring, Rulers And CalipersFTY1Manufactureraccessdata.fda.gov
Unit, Suction OperatoryEBR1Manufactureraccessdata.fda.gov
Unit, Syringe, Air And/Or WaterECB1Manufactureraccessdata.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
May 31, 2006K060172REMA SHAVER BLADESHRXSubstantially EquivalentRema Medizintechnik GmbH.accessdata.fda.gov

Compare with other makers

Updated May 31, 2006. 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.