Molex LLC
United Statesfrom the FDA registration address FDA establishment FEI 3003127839
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Molex LLC makes
Molex LLC manufactures the TeleEnable EMS System, a medical device designed for emergency medical services to facilitate remote patient monitoring and communication during transport.
The TeleEnable EMS System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Telenable Ems System Ref K040663
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003127839
- Address
- 1750 Country Farm Dr, Naperville, IL, 60563
Frequently asked questions
How many devices does MOLEX LLC have in the registry?
The registry currently lists 1 device for MOLEX LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MOLEX LLC's devices?
Among its 1 most recently registered device, MOLEX LLC has devices listed in FDA 510(k) (1 device).
What risk classes do MOLEX LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for MOLEX LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MOLEX LLC in the registry?
The most recently registered devices listed for MOLEX LLC include TELENABLE EMS SYSTEM.