Mega Meditex, Ltd.
IndiaFDA applicant, unverified
- Devices
- 1
What Mega Meditex, Ltd. makes
Mega Meditex, Ltd. manufactures medical devices classified under Class I, including products such as the MEGA MEDITEX LIMITED device. These devices are designed for general medical use, typically involving minimal risk and often serving basic diagnostic, monitoring, or therapeutic functions.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, ensuring compliance with U.S. medical device regulations. Devices are listed in the FDA’s 510(k) clearance registry, and the company operates from the United States.
Catalogue
Mega Meditex Limited Ref K950622
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mega Meditex, Ltd. have in the registry?
The registry currently lists 1 device for Mega Meditex, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mega Meditex, Ltd.'s devices?
Among its 1 most recently registered device, Mega Meditex, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mega Meditex, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mega Meditex, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mega Meditex, Ltd. in the registry?
The most recently registered devices listed for Mega Meditex, Ltd. include MEGA MEDITEX LIMITED.