T.B.S., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What T.B.S., Inc. makes
T.B.S., Inc. manufactures patient movers, which are mechanical devices designed to assist healthcare providers in safely transferring patients between beds, stretchers, and other medical equipment. These devices are engineered to reduce physical strain on caregivers while ensuring patient stability during movement.
The company’s portfolio is classified under FDA Class II devices, requiring premarket notification (510(k)) clearance. These devices are listed in the FDA’s 510(k) registry, adhering to U.S. regulatory standards for medical equipment. The manufacturer operates from the United States.
Catalogue
Patient Mover(Tm) Ref K871582
510(k) 510(k)Patient Mover(Tm) Ref K890555
510(k) 510(k)
Frequently asked questions
How many devices does T.B.S., Inc. have in the registry?
The registry currently lists 2 devices for T.B.S., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T.B.S., Inc.'s devices?
Among its 2 most recently registered devices, T.B.S., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do T.B.S., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for T.B.S., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from T.B.S., Inc. in the registry?
The most recently registered devices listed for T.B.S., Inc. include PATIENT MOVER(TM).