Skip to content

EON MEDITECH PVT. LTD

India IN-MF-000014457 Last updated 21 Oct 2026

Is this your brand? Sign in to claim this brand

Devices
582
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue582

Page 3 of 12

  • Orleon Ref FI1512100

    Class IIa EUDAMED Active

  • Salient Ref PEI1520100

    Class IIa EUDAMED Active

  • Salient Ref PE7165

    Class I EUDAMED Active

  • Orleon Ref F6149L

    Class I EUDAMED Active

  • Osseous Ref EI2160FD

    Class IIa EUDAMED Active

  • Osseous Ref EI1325160L

    Class IIa EUDAMED Active

  • Osseous Ref EI1335120R

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref EI2130TC

    Class IIa EUDAMED Active

  • Salient Ref PE2124B

    Class IIa EUDAMED Active

  • Osseous Ref EI142580

    Class IIa EUDAMEDFDA UDI Active

  • Orleon Ref FI152080

    Class IIa EUDAMED Active

  • Orleon Ref FI1230120

    Class IIa EUDAMED Active

  • Osseous Ref EI152060

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref E3115S

    Class IIa EUDAMED Active

  • Orleon Ref F3111

    Class IIa EUDAMED Active

  • Osseous Ref E3147P

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref E3111236S

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref E7190

    Class I EUDAMEDFDA UDI Active

  • Osseous Ref E7166

    Class I EUDAMEDFDA UDI Active

  • Osseous Ref E7186

    Class I EUDAMEDFDA UDI Active

  • Osseous Ref EI1230150

    Class IIa EUDAMEDFDA UDI Active

  • Salient Ref PE3126

    Class IIa EUDAMED Active

  • Salient Ref PE7181

    Class I EUDAMED Active

  • Salient Ref PE6149M

    Class I EUDAMED Active

  • Orleon Ref FI1240140

    Class IIa EUDAMED Active

  • Orleon Ref FI151470

    Class IIa EUDAMED Active

  • Orleon Ref F2114B

    Class IIa EUDAMED Active

  • Salient Ref PEI1514100

    Class IIa EUDAMED Active

  • Salient Ref PE2137

    Class IIa EUDAMED Active

  • Osseous Ref EI151070

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref EI1220150

    Class IIa EUDAMEDFDA UDI Active

  • Salient Ref PE2137B

    Class IIa EUDAMED Active

  • Orleon Ref F2124B

    Class IIa EUDAMED Active

  • Osseous Ref EI2145SS

    Class IIa EUDAMED Active

  • Osseous Ref E2116

    Class IIa EUDAMED Active

  • Osseous Ref EI1330140L

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref EI141470

    Class IIa EUDAMED Active

  • Osseous Ref EI1220100

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref E2124

    Class IIa EUDAMED Active

  • Osseous Ref EI1350140R

    Class IIa EUDAMED Active

  • Osseous Ref EI1325140R

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref E2137B

    Class IIa EUDAMED Active

  • Orleon Ref F7163

    Class I EUDAMED Active

  • Osseous Ref EI2155SS

    Class IIa EUDAMED Active

  • Osseous Ref EI1240100

    Class IIa EUDAMEDFDA UDI Active

  • Osseous Ref EI1320120R

    Class IIa EUDAMED Active

  • Osseous Ref E2138

    Class IIa EUDAMED Active

  • Osseous Ref EI2115CD

    Class IIa EUDAMED Active

  • Orleon Ref F2117B

    Class IIa EUDAMED Active

  • salient Ref PEI1230140

    Class IIa EUDAMED Active

Showing 101-150 of 582

Related companies

Authorised representatives

What EON MEDITECH PVT. LTD makes

EON Meditech manufactures orthopaedic implants and fixation devices designed for osseous applications, including screws, plates, and related hardware for bone stabilization and reconstruction. Their product line also includes specialized orthopaedic tools and systems for surgical procedures, such as the Salient, Orleon, and other osseous-specific devices.

The company’s portfolio is regulated under EU Medical Device Regulations, with devices classified as Class I, Class IIa, and Class IIb, and is listed in the EUDAMED database. The manufacturer is based in India and adheres to relevant regulatory frameworks for orthopaedic implants and surgical instruments.

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 EON Meditech manufacture?

EON Meditech specializes in orthopaedic implants and fixation devices primarily for osseous (bone-related) applications. Their product line includes screws, plates, and other hardware used in bone stabilization and reconstruction surgeries. Additionally, they produce specialized orthopaedic tools and systems, such as the Salient and Orleon lines, which are designed for surgical procedures involving bone.

Where is EON Meditech based, and what regulatory frameworks do they follow?

EON Meditech is headquartered in India. Their devices are regulated under the EU Medical Device Regulations (MDR) when marketed in the European Union, with classifications spanning Class I, Class IIa, and Class IIb. This classification depends on the risk associated with each specific device, as determined by regulatory authorities.

Are EON Meditech’s devices listed in any regulatory databases?

Yes, EON Meditech’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This database provides transparency on manufacturers, devices, and regulatory information for stakeholders, including healthcare professionals and regulatory bodies.

How are EON Meditech’s devices classified under EU regulations?

EON Meditech’s devices are classified under the EU Medical Device Regulations (MDR) based on their intended purpose and associated risks. For example, osseous implants like screws and plates may fall into Class IIa or Class IIb due to their role in surgical procedures and potential impact on patient safety. Classification ensures appropriate regulatory oversight, with higher-risk devices requiring stricter scrutiny.

What distinguishes EON Meditech’s orthopaedic devices from others in the market?

EON Meditech’s devices are specifically designed for osseous applications, focusing on bone stabilization, reconstruction, and surgical tools tailored for orthopaedic procedures. Their portfolio includes both standard fixation hardware and specialized systems like the Salient and Orleon lines, which are engineered to meet precise clinical needs in orthopaedic surgery. The classification under EU MDR reflects their role in high-risk medical contexts.

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

Information

Country
India
Address
Factory: BL 54, 127, 129, Khanpur Road, Mirapur, Kamrej, Surat -394320, Gujarat, India, Surat, India
PRRC contact
Nirav Khunt
EUDAMED SRN
IN-MF-000014457