Olympia Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Olympia Instruments, Inc. makes
Olympia Instruments, Inc. manufactures the Olympia Faceplate Module, a component designed for medical imaging or procedural applications, and all-in-ear hearing aids for clinical use.
The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Olympia Faceplate Module Ref K896304
Regimes: 510(k) Registry: 510(k)Hearing Aid(All In Ear) Ref K852244
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Olympia Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Olympia Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Olympia Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Olympia Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Olympia Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Olympia Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Olympia Instruments, Inc. in the registry?
The most recently registered devices listed for Olympia Instruments, Inc. include OLYMPIA FACEPLATE MODULE and HEARING AID(ALL IN EAR).