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Data / Medical devices / Germany / Faulhaber Pinzetten KG

Faulhaber Pinzetten KG: FDA-registered device maker in FRITTLINGEN Baden-Wurttemberg, Germany, 2 510(k) clearances

Faulhaber Pinzetten KG is registered with the FDA (registration 8010591) in FRITTLINGEN Baden-Wurttemberg, Germany. It lists 33 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 8, 2019. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Faulhaber Pinzetten KG
FDA registration number
8010591
FEI number
3005649458
Address
Daimlerstr. 1, FRITTLINGEN Baden-Wurttemberg, Germany, 78665
Owner or operator
Faulhaber Pinzetten KG (8010591)
Roles
Contract manufacturer, Manufacturer
First device listed
May 9, 1986
Registered through
2027
Brand names listed
18-1138, J 355-370

Devices it lists

DeviceProduct codeClassRoleSource
Abutment, Implant, Dental, EndosseousNHA2Contract manufactureraccessdata.fda.gov
Accessories, Implant, Dental, EndosseousNDP1Contract manufactureraccessdata.fda.gov
Applier, Surgical, ClipGDO1Contract manufacturer, Manufactureraccessdata.fda.gov
Carrier, Amalgam, OperativeEKI1Contract manufacturer, Manufactureraccessdata.fda.gov
Clamp, Ossicle HoldingJYF1Contract manufacturer, Manufactureraccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Contract manufactureraccessdata.fda.gov
Clamp, VascularDXC2Contract manufactureraccessdata.fda.gov
Curette, EarJYG1Manufactureraccessdata.fda.gov
Curette, Surgical, General UseFZS1Contract manufacturer, Manufactureraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Manufactureraccessdata.fda.gov
ForcepsHTD1Contract manufacturer, Manufactureraccessdata.fda.gov
Forceps, Dressing, DentalEFL1Contract manufacturer, Manufactureraccessdata.fda.gov
Forceps, EntKAE1Contract manufacturer, Manufactureraccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Contract manufacturer, Manufactureraccessdata.fda.gov
Forceps, OphthalmicHNR1Contract manufacturer, Manufactureraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Contract manufacturer, Manufactureraccessdata.fda.gov
HemostatHRQ1Contract manufactureraccessdata.fda.gov
Implant, Endosseous, Root-FormDZE2Contract manufactureraccessdata.fda.gov
Instrument, Ent Manual SurgicalLRC1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Contract manufactureraccessdata.fda.gov
Instrument, MicrosurgicalGZX1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, Surgical, Non-PoweredHAO1Contract manufacturer, Manufactureraccessdata.fda.gov
Instruments, Surgical, CardiovascularDWS1Contract manufacturer, Manufactureraccessdata.fda.gov
Laparoscope, General & Plastic SurgeryGCJ2Contract manufactureraccessdata.fda.gov
Marker, PeriodonticEMP1Contract manufacturer, Manufactureraccessdata.fda.gov
Nasopharyngoscope (Flexible Or Rigid)EOB2Contract manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Contract manufacturer, Manufactureraccessdata.fda.gov
OsteotomeHWM1Contract manufacturer, Manufactureraccessdata.fda.gov
Plier, OrthodonticJEX1Contract manufacturer, Manufactureraccessdata.fda.gov
Pliers, SurgicalHTC1Contract manufacturer, Manufactureraccessdata.fda.gov
Probe And Director, Gastro-UrologyFGM1Contract manufacturer, Manufactureraccessdata.fda.gov
Pusher, Band, OrthodonticECS1Contract manufactureraccessdata.fda.gov
RaspHTR1Contract manufactureraccessdata.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 8, 2019K182773Single-Use Non-Stick Bipolar forceps Bayonet, Single-Use Non-Stick Bipolar Irrigating forceps, Single Use Non-Stick Bipolar Suction forcepsGEISubstantially EquivalentFaulhaber Pinzetten Ohgaccessdata.fda.gov
June 21, 2010K101080NON STICK BIPOLAR FORCEPS MODEL 07/XXX, BIPOLAR FORCEPS MODEL 08/XXX, MONOPOLAR FORCEPS MODEL 09/XXXGEISubstantially EquivalentEgon Faulhaber Surgical Instruments Pinzettenaccessdata.fda.gov

Compare with other makers

Updated October 8, 2019. 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.