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SIGNUS Medizintechnik GmbH

US

Last updated May 24, 2026

What SIGNUS Medizintechnik GmbH makes

SIGNUS Medizintechnik GmbH manufactures reusable orthopaedic surgical kits and spinal fixation hardware, including non-bioabsorbable bone screws, metallic and polymeric interbody fusion cages, internal fixation rods, connectors, hooks, and spinal plates. Their portfolio also includes spinal fixation systems designed for internal stabilization, such as the COSY, DIPLOMAT, and RABEA series, as well as specialized implants like the TASMIN R and TETRIS II 4°.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does SIGNUS Medizintechnik GmbH primarily manufacture?

SIGNUS Medizintechnik GmbH specializes in orthopaedic surgical procedure kits and spinal fixation hardware. Their portfolio includes reusable non-medicated kits, as well as devices like non-bioabsorbable bone screws, metallic and polymeric spinal interbody fusion cages, internal spinal fixation rods, connectors, hooks, and non-bioabsorbable spinal plates. These products are designed for spinal stabilization and fusion procedures.

Where is SIGNUS Medizintechnik GmbH based?

SIGNUS Medizintechnik GmbH operates from the United States. The company’s headquarters and manufacturing operations are located within the country, though specific regional offices or production sites may vary.

Which regulatory registries list SIGNUS Medizintechnik GmbH’s devices?

SIGNUS Medizintechnik GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices authorized under FDA regulations, including those classified under Class I and Class II categories.

How are SIGNUS Medizintechnik GmbH’s devices classified under FDA regulations?

SIGNUS Medizintechnik GmbH’s devices fall into two primary FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and clinical benefits.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
signus.com
LinkedIn
—
Facebook
—
Phone
+49602391660
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
344203948

Catalogue (5251)

Page 3 of 106
DeviceModel / ReferenceRegistriesClassStatus
Cylox St Locking screw, cage
FDA UDI
Class IIActive
Diplomat Pedicle screw, fenestrated, monoaxial
FDA UDI
Class IIActive
Tetris 4° Lumbar cage, angled
FDA UDI
Class IIActive
Cosy Shank screw with tulip, cannulated, polyaxial
FDA UDI
Class IIActive
Semial Graft loading platform
FDA UDI
Class IActive
Diplomat Screwdriver, set screw
FDA UDI
Class IActive
Diplomat Pedicle screw w/o tulip for VB-fractures, cannulated, polyaxial
FDA UDI
Class IIActive
Mobis Xl 0° Lumbar cage, straight
FDA UDI
Class IIActive
Tetris St 0° Lumbar cage, straight
FDA UDI
Class IIActive
Nubic Rasp
FDA UDI
Class IActive
Diplomat Tap
FDA UDI
Class IActive
Mobis Ii 5° Lumbar cage, angled
FDA UDI
Class IIActive
Tetris 0° Lumbar cage, straight
FDA UDI
Class IIActive
Cosy Parallel connector closed
FDA UDI
Class IIActive
Cosy Rod, straight
FDA UDI
Class IIActive
Tetris St 20° Lumbar cage, angled
FDA UDI
Class IIActive
Conklusion Pedicle screw
FDA UDI
Class IIActive
Cosy Rod, curved
FDA UDI
Class IIActive
Tasmin R Inserter, T-handle
FDA UDI
Class IActive
Cosy Screw with tulip, angled, cannulated, polyaxial, self drilling, incl. set screw
FDA UDI
Class IIActive
Tetris 0° Lumbar cage, straight
FDA UDI
Class IIActive
Monopoly Tray, lid
FDA UDI
Class IActive
Tetris St Trial
FDA UDI
Class IActive
Tetris St Disctractor, paddle
FDA UDI
Class IActive
Tetris St Disctractor, paddle
FDA UDI
Class IActive
Cosy Shank screw with tulip, cannulated, polyaxial
FDA UDI
Class IIActive
Diplomat Ft Pedicle screw, fenestrated, monoaxial
FDA UDI
Class IIActive
Diplomat Pedicle screw w/o tulip, fenestrated, polyaxial
FDA UDI
Class IIActive
Diplomat Tray, insert, implants
FDA UDI
Class IActive
Noval Trial
FDA UDI
Class IActive
Tosca Cervical plate, 1-level
FDA UDI
Class IIActive
Semial 5° Lumbar cage, angled
FDA UDI
Class IIActive
Rabea 0° Cervical cage, straight
FDA UDI
Class IIActive
Cosy Shank screw with tulip, polyaxial, incl. set screw
FDA UDI
Class IIActive
Cosy Shank screw with tulip, cannulated, polyaxial, incl. set screw
FDA UDI
Class IIActive
Tetris 0° Lumbar cage, straight
FDA UDI
Class IIActive
Rabea 0° Cervical cage, straight
FDA UDI
Class IIActive
Cosy Screw with tulip, angled, polyaxial, self drilling
FDA UDI
Class IIActive
Diplomat Screwdriver, set screw
FDA UDI
Class IActive
Rabea Inserter
FDA UDI
Class IActive
Tetris St Trial
FDA UDI
Class IActive
Sacronail Screw plug
FDA UDI
Class IIActive
Tosca Ii Awl
FDA UDI
Class IActive
Diplomat Pedicle screw, fenestrated, reduction, monoaxial, incl. set screw
FDA UDI
Class IIActive
Cosy Occipital screw
FDA UDI
Class IIActive
Diplomat Pedicle screw, fenestrated, reduction, monoaxial
FDA UDI
Class IIActive
Diplomat Pedicle screw, fenestrated, reduction, monoaxial, incl. set screw
FDA UDI
Class IIActive
Cosy Occipital screw
FDA UDI
Class IIActive
Mobis Xl 0° Lumbar cage, straight
FDA UDI
Class IIActive
Sacronail Instrument guide
FDA UDI
Class IIActive

Related Companies

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Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Signus Medizintechnik Gmbh ALZENAU Bavaria · DE FEI 1000615957