Boxout, LLC
Country not established
- Devices
- 113
What Boxout, LLC makes
Boxout, LLC manufactures single-use transcutaneous electrical stimulation electrodes, manual scalpel blades, and nitrile examination gloves. Their portfolio also includes physical therapy neuromuscular stimulation systems, external electric-heating pads for temperature regulation, and drug-delivery iontophoresis patches. Additionally, they produce benchtop therapeutic agent nebulizers and single-use nebulizing system delivery sets.
The company’s devices are classified under FDA regulations as Class I or Class II and are listed in the FDA’s Unique Device Identifier (UDI) database. Boxout, LLC operates from the United States.
Catalogue
Search and filter all 113 devicesShowing 1-50 of 113
Company details
- DUNS number
- 066689993
- Phone
- 866-528-2152
Frequently asked questions
How many devices does BOXOUT, LLC have in the registry?
The registry currently lists 113 devices for BOXOUT, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list BOXOUT, LLC's devices?
Among its 50 most recently registered devices, BOXOUT, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do BOXOUT, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for BOXOUT, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BOXOUT, LLC in the registry?
The most recently registered devices listed for BOXOUT, LLC include BodyMed BDMCSBS10SAM, BodyMed ZZHP1427, BodyMed ZZHP1414 and BODYMED NPP9375R.