Retlif, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Retlif, Inc. makes
Retlif, Inc. manufactures hearing instruments, including Bosch-branded devices, and a blood pressure monitor designed for clinical or home use. These products are intended for diagnostic and monitoring purposes in audiological and cardiovascular assessments.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Bosch Hearing Instruments Ref K812503
Regimes: 510(k) Registry: 510(k)Tonotest Blood Pressure Monitor Ref K800904
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retlif, Inc. have in the registry?
The registry currently lists 2 devices for Retlif, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retlif, Inc.'s devices?
Among its 2 most recently registered devices, Retlif, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Retlif, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Retlif, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retlif, Inc. in the registry?
The most recently registered devices listed for Retlif, Inc. include BOSCH HEARING INSTRUMENTS and TONOTEST BLOOD PRESSURE MONITOR.