Telesonic, Inc.
United StatesFDA applicant, unverified
- Devices
- 12
What Telesonic, Inc. makes
Telesonic, Inc. manufactures custom-in-the-ear hearing aids and post-auricular hearing aid models, including specific variants such as the P-101, S-101, and ASP-103. Their portfolio also includes body stimulators and branded hearing aid systems like the Telesonic V-101, Telesonic & Arcon, and combinations with Soundex and generic models.
The company’s devices are classified under FDA categories Class I and Class II, with several listed in the FDA’s 510(k) premarket notification registry. These products are regulated under U.S. medical device laws, and the manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Telesonic, Inc. have in the registry?
The registry currently lists 12 devices for Telesonic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telesonic, Inc.'s devices?
Among its 12 most recently registered devices, Telesonic, Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do Telesonic, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Telesonic, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telesonic, Inc. in the registry?
The most recently registered devices listed for Telesonic, Inc. include CUSTOM-IN-THE-EAR HEARING AID, TELESONIC BODY STIMULATOR, POST-AURICULAR HEARING AID MODEL P-101 and TELESONIC (HEARING AID).