Telstar Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Telstar Electronics, Inc. makes
Telstar Electronics, Inc. manufactures a range of in-the-ear (ITE) hearing aids, including custom-molded models such as the Full Shell ITE and pre-wired hearing aids designed for direct acoustic coupling. Their portfolio includes rechargeable and non-rechargeable devices, such as the Model PP, F3TS, and C series, tailored for various hearing loss profiles. Additional offerings include specialized ITE hearing aids like the Model 1/3 and Model 0/3, which cater to specific auditory needs.
The company’s devices are classified under FDA categories Class I and Class II, with relevant products listed via the 510(k) pathway. Their hearing aids are registered in the FDA’s 510(k) database, reflecting their regulatory compliance. The manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Telstar Electronics, Inc. have in the registry?
The registry currently lists 11 devices for Telstar Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telstar Electronics, Inc.'s devices?
Among its 11 most recently registered devices, Telstar Electronics, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Telstar Electronics, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Telstar Electronics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telstar Electronics, Inc. in the registry?
The most recently registered devices listed for Telstar Electronics, Inc. include TELSTAR MODEL PP ITE HEARING AID, TELSTAR MODEL PP, TELSTAR MODEL F3TS HEARING AID and TELSTAR MODEL F ITE HEARING AID.