Bodylog, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Bodylog, Inc. makes
Bodylog, Inc. manufactures therapeutic electromyographic devices, including the Bodylog 500 RET system, as well as stress reduction packages designed to deliver targeted muscle stimulation for relaxation and pain management.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Bodylog Stress Reduction Package Ref K873418
Regimes: 510(k) Registry: 510(k)Bodylog Enhanced Stress Reduction Package Ref K902450
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bodylog, Inc. have in the registry?
The registry currently lists 3 devices for Bodylog, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bodylog, Inc.'s devices?
Among its 3 most recently registered devices, Bodylog, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bodylog, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bodylog, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bodylog, Inc. in the registry?
The most recently registered devices listed for Bodylog, Inc. include THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS, BODYLOG STRESS REDUCTION PACKAGE and BODYLOG ENHANCED STRESS REDUCTION PACKAGE.