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TENORTHO SRL

Italy IT-MF-000050082 Last updated 21 Oct 2026

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Devices
428
Registries
EUDAMED
FDA recalls
0

Catalogue428

Page 1 of 9

  • TO4103 Ref TO4103_XS

    Class I EUDAMED Active

  • TO3100 Ref TO3100_M

    Class I EUDAMED Active

  • TO1106 Ref TO1106_L

    Class I EUDAMED Active

  • TO2207N Ref TO2207N_SSX

    Class I EUDAMED Active

  • TO2209 Ref TO2209_SDX

    Class I EUDAMED Active

  • TO3112 Ref TO3112_S

    Class I EUDAMED Active

  • TO4302C_EE Ref TO4302C_MSX_EE

    Class I EUDAMED Active

  • TO3120 Ref TO3120_M

    Class I EUDAMED Active

  • TO2115 Ref TO2115_1SX

    Class I EUDAMED Active

  • TO3105N Ref TO3105N_XS

    Class I EUDAMED Active

  • TO3111 Ref TO3111_XS

    Class I EUDAMED Active

  • TO2304 Ref TO2304_2

    Class I EUDAMED Active

  • TO1305 Ref TO1305_XS

    Class I EUDAMED Active

  • TO3104N Ref TO3104N_XLDX

    Class I EUDAMED Active

  • TO3102N Ref TO3102N_XS

    Class I EUDAMED Active

  • TO3118 Ref TO3118_L

    Class I EUDAMED Active

  • TO1205 Ref TO1205_XXL

    Class I EUDAMED Active

  • TO0100 Ref TO0100_S6

    Class I EUDAMED Active

  • TO4303 Ref TO4303_MSX

    Class I EUDAMED Active

  • TO2206N Ref TO2206N_LDX

    Class I EUDAMED Active

  • TO3104N Ref TO3104N_LDX

    Class I EUDAMED Active

  • TO1200 Ref TO1200_XXXL

    Class I EUDAMED Active

  • TO2302 Ref TO2302_4

    Class I EUDAMED Active

  • TO1301 Ref TO1301_S

    Class I EUDAMED Active

  • TO1308MG Ref TO1308_2_O

    Class I EUDAMED Active

  • TO1103 Ref TO1103_S

    Class I EUDAMED Active

  • TO2208N Ref TO2208N_SDX

    Class I EUDAMED Active

  • TO2301 Ref TO2301_XLSX

    Class I EUDAMED Active

  • TO1206 Ref TO1206_XL

    Class I EUDAMED Active

  • TO2301 Ref TO2301_LSX

    Class I EUDAMED Active

  • TO3310 Ref TO3310_MSX

    Class I EUDAMED Active

  • TO2210 Ref TO2210_XXLDX

    Class I EUDAMED Active

  • TO2210 Ref TO2210_MDX

    Class I EUDAMED Active

  • TO2114 Ref TO2114_1DX

    Class I EUDAMED Active

  • TO2216 Ref TO2216_XS

    Class I EUDAMED Active

  • TO1305 Ref TO1305_L

    Class I EUDAMED Active

  • TO3100 Ref TO3100_XL

    Class I EUDAMED Active

  • TO1203 Ref TO1203_M

    Class I EUDAMED Active

  • TO0100 Ref TO0100_M6

    Class I EUDAMED Active

  • TO2302 Ref TO2302_6

    Class I EUDAMED Active

  • TO3107N Ref TO3107N_XS

    Class I EUDAMED Active

  • TO1205 Ref TO1205_L

    Class I EUDAMED Active

  • TO4104P Ref TO4104P_XL

    Class I EUDAMED Active

  • TO2303 Ref TO2303_2

    Class I EUDAMED Active

  • TO1308MG Ref TO1308_1_O

    Class I EUDAMED Active

  • TO3102N Ref TO3102N_XL

    Class I EUDAMED Active

  • TO1205 Ref TO1205_XXXL

    Class I EUDAMED Active

  • TO4305 Ref TO4305_S

    Class I EUDAMED Active

  • TO2210 Ref TO2210_LSX

    Class I EUDAMED Active

  • TO3310 Ref TO3310_LSX

    Class I EUDAMED Active

Showing 1-50 of 428

About

People, doctors, orthopaedia: in the concept of Tenortho constitute a system, an alliance in which everyone’s role is complementary to that of others:

Translated from the manufacturer's own website. Source

What TENORTHO SRL makes

Tenortho Srl manufactures a range of Class I medical devices, including orthopaedic and trauma-related products such as fixation systems, surgical screws, and orthopaedic implants. Their portfolio includes devices like TO3118, TO2302, and TO1305, which are designed for bone stabilization and fracture fixation in orthopaedic procedures.

These devices are listed under the EU Medical Device Regulation via the eudamed database, adhering to Class I regulatory requirements. The company is based in Italy and ensures compliance with EU medical device regulations for each authorised product.

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 Tenortho SRL manufacture?

Tenortho SRL specialises in Class I medical devices primarily focused on orthopaedic and trauma care. Their portfolio includes fixation systems, surgical screws, and orthopaedic implants, such as TO3118, TO2302, and TO1305, which are designed for bone stabilisation and fracture fixation during surgical procedures.

Where is Tenortho SRL based, and what regulatory framework do its devices follow?

Tenortho SRL is based in Italy. Their devices are authorised under the EU Medical Device Regulation (MDR) and are listed in the eudamed database, which is the official EU registry for medical devices. Since their products fall under Class I classification, they must comply with the specific regulatory requirements for this category.

Are Tenortho SRL’s devices listed in any regulatory registries, and why does this matter?

Yes, Tenortho SRL’s devices are listed in the eudamed database, the EU’s central registry for medical devices. This listing ensures transparency and traceability, allowing healthcare professionals, regulators, and patients to verify the device’s authorised status and compliance with EU medical device regulations. Listing in eudamed is mandatory for all devices placed on the EU market.

How are Tenortho SRL’s devices classified under EU regulations, and what does this classification mean?

Tenortho SRL’s devices are classified as Class I under the EU Medical Device Regulation. This classification is determined by factors like the device’s intended use, duration of contact with the body, and potential risks. Class I devices are generally considered low-risk, but they still must meet essential safety and performance requirements to ensure their safe and effective use in clinical settings.

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

Information

Country
Italy
Address
100, VIA TRENTO E TRIESTE, BIASSONO, Italy
Phone
+39 0398943960
PRRC contact
ALESSIO TENTORIO
EUDAMED SRN
IT-MF-000050082