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Data / Medical devices / Germany / Hermann Medizintechnik GMBH

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

Hermann Medizintechnik GMBH is registered with the FDA (registration 8010257) in FRIDINGEN Baden-Wurttemberg, Germany. It lists 69 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 29, 2005. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
8010257
FEI number
4498
Address
Wuerttemberger Strasse 26, FRIDINGEN Baden-Wurttemberg, Germany, 78567
Owner or operator
Hermann GmbH (8010257)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
March 9, 1978
Registered through
2027
Brand names listed
11 - 0043 - LOCKLIN scissors, straight, angled,, 11-0043-1 - LOCKLIN scissors, angled,, 11-0043-1 - LOCKLIN scissors, cvd., 6 1/4",16cm, 11-0043-2 - LOCKLIN scissors, straight, 6 1/4",16cm, 11-0049 - GOLDMANN-FOX Scissors, saw edge,, 11-0050 - GOLDMANN-FOX scissors, straight,, 11-0051 - GOLDMANN-FOX scissors, curved,, 11-0053 - Gums Scissors, curved, sharp/sharp, and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, ArthroscopicNBH1Contract manufacturer, Manufactureraccessdata.fda.gov
Accessories, Cleaning Brushes, For EndoscopeMNL1Contract manufactureraccessdata.fda.gov
Applier, Surgical, ClipGDO1Manufactureraccessdata.fda.gov
Bit, DrillHTW1Contract manufactureraccessdata.fda.gov
Blade, Saw, General & Plastic Surgery, SurgicalGFA1Manufactureraccessdata.fda.gov
Blade, ScalpelGES1Manufactureraccessdata.fda.gov
Camera, Cine, Endoscopic, With AudioFTS1Manufactureraccessdata.fda.gov
Cerclage, FixationJDQ2Contract manufactureraccessdata.fda.gov
Chisel (Osteotome)KDG1Manufactureraccessdata.fda.gov
Chisel, Surgical, ManualFZO1Manufactureraccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Manufactureraccessdata.fda.gov
Curette, Surgical, General UseFZS1Manufactureraccessdata.fda.gov
Cutter, WireHXZ1Manufactureraccessdata.fda.gov
Dilator, Esophageal, EntKCF1Manufactureraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Contract manufacturer, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Elevator, Surgical, General & Plastic SurgeryGEG1Manufactureraccessdata.fda.gov
Endoscope, Ac-Powered And AccessoriesGCP2Contract manufactureraccessdata.fda.gov
Evacuator, Bladder, Manually OperatedFFD1Manufactureraccessdata.fda.gov
ForcepsHTD1Manufactureraccessdata.fda.gov
Forceps, Biopsy, GynecologicalHFB1Manufactureraccessdata.fda.gov
Forceps, EntKAE1Manufactureraccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Manufactureraccessdata.fda.gov
Forceps, OphthalmicHNR1Manufactureraccessdata.fda.gov
Forceps, Rongeur, SurgicalEMH1Manufactureraccessdata.fda.gov
Gauge, DepthHTJ1Contract manufactureraccessdata.fda.gov
Guide, Surgical, InstrumentFZX1Contract manufacturer, Manufactureraccessdata.fda.gov
Hammer, SurgicalFZY1Manufactureraccessdata.fda.gov
Handle, ScalpelGDZ1Manufactureraccessdata.fda.gov
HemostatHRQ1Manufactureraccessdata.fda.gov
Holder, Needle, GastroenterologicFHQ1Manufactureraccessdata.fda.gov
Hook, Surgical, General & Plastic SurgeryGDG1Manufactureraccessdata.fda.gov
Hook, TrachealKCH1Manufactureraccessdata.fda.gov
Hysteroscope AccessoriesNWW1Manufactureraccessdata.fda.gov
Instrument, Ent Manual SurgicalLRC1Manufactureraccessdata.fda.gov
Instrument, Hand, Calculus RemovalELA1Manufactureraccessdata.fda.gov
Instrument, Manual, General Obstetric-GynecologicKOH1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, MicrosurgicalGZX1Manufactureraccessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE1Contract manufactureraccessdata.fda.gov
Instruments, Surgical, CardiovascularDWS1Manufactureraccessdata.fda.gov
Knife, SurgicalEMF1Manufactureraccessdata.fda.gov
Laparoscope, General & Plastic SurgeryGCJ2Contract manufacturer, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Mediastinoscope, SurgicalEWY2Contract manufactureraccessdata.fda.gov
Needle, Aspiration And Injection, ReusableGDM1Manufactureraccessdata.fda.gov
Needle, Suturing, ReusableGDL1Manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Contract manufacturer, Manufactureraccessdata.fda.gov
Plate, Fixation, BoneHRS2Contract manufactureraccessdata.fda.gov
ProbeHXB1Manufactureraccessdata.fda.gov
Prosthesis, Toe, Hemi-, PhalangealKWD2Contract manufactureraccessdata.fda.gov
Punch, SurgicalLRY1Manufactureraccessdata.fda.gov
RaspHTR1Manufactureraccessdata.fda.gov
RetractorGAD1Manufactureraccessdata.fda.gov
Retractor, All TypesEIG1Manufactureraccessdata.fda.gov
RongeurHTX1Manufactureraccessdata.fda.gov
Saw, Manual And AccessoriesGDR1Manufactureraccessdata.fda.gov
Scissors, General, SurgicalLRW1Manufactureraccessdata.fda.gov
Scissors, Medical, DisposableJOK1Manufactureraccessdata.fda.gov
Scissors, OphthalmicHNF1Manufactureraccessdata.fda.gov
Scissors, Orthopedic, SurgicalHRR1Manufactureraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Manufactureraccessdata.fda.gov
Screw, Fixation, BoneHWC2Contract manufactureraccessdata.fda.gov
Speculum, EntEPY1Manufactureraccessdata.fda.gov
Speculum, Vaginal, MetalHDF1Manufactureraccessdata.fda.gov
Staple, Fixation, BoneJDR2Contract manufactureraccessdata.fda.gov
Stimulator, Caloric-AirKHH1Manufactureraccessdata.fda.gov
Tape, Measuring, Rulers And CalipersFTY1Manufactureraccessdata.fda.gov
TemplateHWT1Contract manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Manufactureraccessdata.fda.gov
Trocar, EntKTE1Manufactureraccessdata.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
July 29, 2005K051610HANS HERMANN LAPAROSCOPES AND ACCESSORIESGCJSubstantially EquivalentHans Hermann GmbHaccessdata.fda.gov

Compare with other makers

Updated July 29, 2005. 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.