EON MEDITECH PVT. LTD
India IN-MF-000014457 Last updated 21 Oct 2026
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- Devices
- 582
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
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Osseous Ref E7181
Orleon Ref F7178
Osseous Ref E7184
Osseous Ref E3148FSP
Orleon Ref F6149L
Osseous Ref E2124B
Orleon Ref FI151470
Osseous Ref EI1230160
Salient Ref PEI1507100
Osseous Ref EI2115TC
Osseous Ref EI1220160
Osseous Ref EI0968
Salient Ref PEI1220140
Salient Ref PEI1240160
Salient Ref PEI1240140
Osseous Ref E3131218
Osseous Ref E2117
Orleon Ref FI150780
Osseous Ref EI150870
Salient Ref PEI0968
Osseous Ref E3146NS
Orleon Ref F7181
Osseous Ref EI140480
Osseous Ref EI1240120
Osseous Ref E7170
Osseous Ref EI2130CD
Orleon Ref F2112
Salient Ref PE7169
Osseous Ref EI2120TC
Osseous Ref EI150480
Salient Ref PE7162
Osseous Ref EI2120SS
Osseous Ref EI2204
Osseous Ref EI1320140L
Osseous Ref E2113B
Osseous Ref EI1325160R
Orleon Ref F7181
Osseous Ref EI2170TC
Salient Ref PE7188
Orleon Ref F2113B
Orleon Ref FI1516100
Osseous Ref E3110936S
Osseous Ref E3148FTP
salient Ref PEI1516100
Osseous Ref EI1240160
Salient Ref PEI152080
Osseous Ref EI151080
Osseous Ref EI2125TC
Orleon Ref FI142580
Orleon Ref F2125
Showing 51-100 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