US Hearing Centers, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What US Hearing Centers, Inc. makes
Us Hearing Centers, Inc. manufactures custom in-the-ear (ITE) and in-the-canal (ITC) prescription hearing aids, including models such as the LP, PP+, and CA/C series. These devices are designed for behind-the-ear (BTE) fitting with ear tips or molds for personalized hearing amplification.
The company’s products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. These devices are listed in the FDA’s 510(k) database and comply with U.S. regulatory requirements for hearing aids.
Catalogue
Ite Prescription Series Model LP Ref K891915
Regimes: 510(k) Registry: 510(k)Ite Prescription Series Model Pp + F Ref K891916
Regimes: 510(k) Registry: 510(k)Itc Prescription Series Model Ca And C Ref K891914
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Us Hearing Centers, Inc. have in the registry?
The registry currently lists 3 devices for Us Hearing Centers, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Us Hearing Centers, Inc.'s devices?
Among its 3 most recently registered devices, Us Hearing Centers, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Us Hearing Centers, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Us Hearing Centers, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Us Hearing Centers, Inc. in the registry?
The most recently registered devices listed for Us Hearing Centers, Inc. include ITE PRESCRIPTION SERIES MODEL LP, ITE PRESCRIPTION SERIES MODEL PP + F and ITC PRESCRIPTION SERIES MODEL CA AND C.