Choice Therapeutics
Country not established
- Devices
- 1
What Choice Therapeutics makes
Choice Therapeutics manufactures Therabond Antimicrobial Barrier Systems, designed as protective barriers to reduce microbial contamination in medical and surgical settings. These systems are intended for use in wound care, surgical drapes, and other clinical applications where infection prevention is critical.
The company’s portfolio is regulated under FDA Class II (U) devices and requires 510(k) clearance in the United States. The products are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Therabond Antimicrobial Barrier Systems Ref K073213
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Choice Therapeutics have in the registry?
The registry currently lists 1 device for Choice Therapeutics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Choice Therapeutics's devices?
Among its 1 most recently registered device, Choice Therapeutics has devices listed in FDA 510(k) (1 device).
What are the newest devices from Choice Therapeutics in the registry?
The most recently registered devices listed for Choice Therapeutics include THERABOND ANTIMICROBIAL BARRIER SYSTEMS.