EON MEDITECH PVT. LTD
India IN-MF-000014457 Last updated 21 Oct 2026
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- Devices
- 582
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Osseous Ref E7182
Orleon Ref F6149S
Osseous Ref E3110955S
Osseous Ref E3111055F
Orleon Ref FI1830150
Salient Ref PE3115M
Osseous Ref EI1340140L
Orleon Ref FI1230120
Osseous Ref E3111055S
Osseous Ref EI1340120L
Salient Ref PE2123
Osseous Ref EI1507100
Salient Ref PEI1508100
Osseous Ref E2128
Osseous Ref EI151270
Osseous Ref EI1340120R
Orleon Ref FI150770
Osseous Ref EI2105FD
Osseous Ref EI1420100
Orleon Ref F7170
Osseous Ref E7163
Osseous Ref EI1230140
Osseous Ref EI2202
Osseous Ref E3111255S
Osseous Ref E3110955S
Salient Ref PEI1250140
Osseous Ref EI2145CD
Osseous Ref EI1240100
Q0399 Ref EI151470
Osseous Ref E2114BW
Osseous Ref EI1320120R
Osseous Ref E21132W
Orleon Ref F2125B
Salient Ref PEI150780
Salient Ref PE5150L
Osseous Ref EI2135FD
Osseous Ref EI1335120L
Osseous Ref EI1320160L
Osseous Ref E3148FSP
Osseous Ref E3146NS
Orleon Ref FI150670
Osseous Ref EI141480
Osseous Ref EI2105SS
Osseous Ref EI141470
Osseous Ref EI2155TC
Osseous Ref E2109
Osseous Ref E2117
Orleon Ref FI151270
Osseous Ref EI1825150
Salient Ref PE3148FT
Showing 201-250 of 582
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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.
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.
Information
- Country
- India
- Address
- Factory: BL 54, 127, 129, Khanpur Road, Mirapur, Kamrej, Surat -394320, Gujarat, India, Surat, India
- Website
- www.eonmeditech.com
- [email protected]
- PRRC contact
- Nirav Khunt
- EUDAMED SRN
- IN-MF-000014457