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Data / Medical devices / Germany / SMT Schilling Metalltechnik GMBH

SMT Schilling Metalltechnik GMBH: FDA-registered device maker in MUHLHEIM Baden-Wurttemberg, Germany, 1 510(k) clearance

SMT Schilling Metalltechnik GMBH is registered with the FDA (registration 9680619) in MUHLHEIM Baden-Wurttemberg, Germany. It lists 37 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 5, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9680619
FEI number
3001026312
Address
Gries Weg 33, MUHLHEIM Baden-Wurttemberg, Germany, 78570
Owner or operator
SMT SCHILLING METALLTECHNIK GMBH (9010184)
Roles
Contract manufacturer, Manufacturer
First device listed
April 15, 1994
Registered through
2026
Brand names listed
01-1071-015 CANNULATED COUNTERSINK 8 MM, Depth Gauge, Guide Wire, Kirschner Wire, Steinmann Pin

Devices it lists

DeviceProduct codeClassRoleSource
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT2Contract manufactureraccessdata.fda.gov
BenderHXW1Manufactureraccessdata.fda.gov
Bit, DrillHTW1Contract manufactureraccessdata.fda.gov
Bone MillLYS1Contract manufacturer, Manufactureraccessdata.fda.gov
CaliperKTZ1Manufactureraccessdata.fda.gov
Cannula, Surgical, General & Plastic SurgeryGEA1Contract manufacturer, Manufactureraccessdata.fda.gov
ClampHXD1Manufactureraccessdata.fda.gov
Cutter, SurgicalFZT1Manufactureraccessdata.fda.gov
Cutter, WireHXZ1Manufactureraccessdata.fda.gov
ForcepsHTD1Contract manufacturer, Manufactureraccessdata.fda.gov
ForkHXE1Contract manufactureraccessdata.fda.gov
Gauge, DepthHTJ1Contract manufacturer, Manufactureraccessdata.fda.gov
Guide, Surgical, InstrumentFZX1Contract manufactureraccessdata.fda.gov
Instrument, Bending Or ContouringHXP1Contract manufacturer, Manufactureraccessdata.fda.gov
Instrument, Cutting, OrthopedicHTZ1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Contract manufactureraccessdata.fda.gov
Instrument, Surgical, Non-PoweredHAO1Manufactureraccessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE1Contract manufactureraccessdata.fda.gov
MalletHXL1Contract manufactureraccessdata.fda.gov
Needle, Suturing, ReusableGDL1Contract manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Contract manufactureraccessdata.fda.gov
Passer, Wire, OrthopedicHXI1Contract manufactureraccessdata.fda.gov
Pin, Fixation, SmoothHTY2Contract manufactureraccessdata.fda.gov
Pin, Fixation, ThreadedJDW2Contract manufactureraccessdata.fda.gov
Plate, Fixation, BoneHRS2Contract manufactureraccessdata.fda.gov
Plier, OrthodonticJEX1Manufactureraccessdata.fda.gov
Pliers, SurgicalHTC1Manufactureraccessdata.fda.gov
ProbeHXB1Contract manufactureraccessdata.fda.gov
Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-ConstrainedJWJ2Contract manufactureraccessdata.fda.gov
RetractorGAD1Manufactureraccessdata.fda.gov
Screw, Fixation, BoneHWC2Contract manufacturer, Manufactureraccessdata.fda.gov
ScrewdriverHXX1Contract manufacturer, Manufactureraccessdata.fda.gov
Stylet, Surgical, General & Plastic SurgeryGAH1Contract manufactureraccessdata.fda.gov
Sucker, Cardiotomy Return, Cardiopulmonary BypassDTS2Contract manufactureraccessdata.fda.gov
Twister, WireHXS1Manufactureraccessdata.fda.gov
Washer, Bolt NutHTN2Manufactureraccessdata.fda.gov
WrenchHXC1Contract manufacturer, 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
April 5, 2013K124027MONSTER SCREW SYSTEMHWCSubstantially EquivalentApogee Orthosolutionsaccessdata.fda.gov

Compare with other makers

Updated April 5, 2013. 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.